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Occlusive Dressing

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61. Role of Surgical Dressings in Total Joint Arthroplasty: A Randomized Controlled Trial. (Abstract)

Role of Surgical Dressings in Total Joint Arthroplasty: A Randomized Controlled Trial. We conducted a randomized controlled trial to compare efficacy of an occlusive antimicrobial barrier dressing and a standard surgical dressing in patients who underwent primary total joint arthroplasty. Two hundred sixty-two patients were randomized to receive either an occlusive dressing or a standard dressing. Wounds were closed in identical fashion. Outcomes included wound complications, dressing changes (...) , and patient satisfaction. With use of occlusive dressing (vs standard dressing), wound complications (including skin blistering) were significantly (P = 0.15) reduced; there were significantly (P < .0001) fewer dressing changes; and patient satisfaction was significantly (P < .0001) higher. Use of occlusive dressings can reduce wound complications and promote wound healing after total joint arthroplasty.

2015 American journal of orthopedics (Belle Mead, N.J.) Controlled trial quality: uncertain

62. Impact of Timing of Wound Dressing Removal After Cesarean Section

, and re-epithelialization is thought to occur within 24 to 48 hours. Early studies into wound care demonstrated that dressings influence the repair process. The post-operative wound dressing acts to ensure the wound bed stays moist, decrease pain and inflammation, and improve scar appearance. Additionally, occlusive dressings increase the rate of re-epithelialization post-operatively compared to those wounds left open. The importance of dressings has been established, but the ideal time (...) that postoperative dressings should remain in place remains elusive. Studies have shown that early removal of dressings (6 hours after wounding) markedly decreases the rate of resurfacing, while leaving the bandage on for greater than 48 hours produced no greater benefit. The United States Centers for Disease Control and Prevention recommends that the sterile dressing stay in place for 24-48 hours post-operatively on an incision that has been closed by primary intention. Although the window of benefit provided

2015 Clinical Trials

63. Standard Versus PICO Dressings in Lower-Extremity Bypass Patients

Infection Wound Dressing Negative Pressure Wound Dressing Additional relevant MeSH terms: Layout table for MeSH terms Cardiovascular Diseases Vascular Diseases Peripheral Arterial Disease Peripheral Vascular Diseases Atherosclerosis Arteriosclerosis Arterial Occlusive Diseases (...) Standard Versus PICO Dressings in Lower-Extremity Bypass Patients Standard Versus PICO Dressings in Lower-Extremity Bypass Patients - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save this study Warning You have reached the maximum number of saved studies (100). Please remove one or more studies before adding more. Standard Versus PICO

2015 Clinical Trials

64. Comparison of Prevena Negative Pressure Incision Management System vs. Standard Dressing After Vascular Surgery

Comparison of Prevena Negative Pressure Incision Management System vs. Standard Dressing After Vascular Surgery Comparison of Prevena Negative Pressure Incision Management System vs. Standard Dressing After Vascular Surgery - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save this study Warning You have reached the maximum number of saved (...) studies (100). Please remove one or more studies before adding more. Comparison of Prevena Negative Pressure Incision Management System vs. Standard Dressing After Vascular Surgery The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. of clinical studies and talk to your health care provider before participating. Read our for details. ClinicalTrials.gov

2015 Clinical Trials

65. Combination of a Polymeric Membrane Dressing Plus Negative Pressure Wound Therapy Against Negative Pressure Wound Therapy Alone

Combination of a Polymeric Membrane Dressing Plus Negative Pressure Wound Therapy Against Negative Pressure Wound Therapy Alone Combination of a Polymeric Membrane Dressing Plus Negative Pressure Wound Therapy Against Negative Pressure Wound Therapy Alone - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save this study Warning You have reached (...) the maximum number of saved studies (100). Please remove one or more studies before adding more. Combination of a Polymeric Membrane Dressing Plus Negative Pressure Wound Therapy Against Negative Pressure Wound Therapy Alone The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our for details. ClinicalTrials.gov Identifier: NCT02399722 Recruitment Status

2015 Clinical Trials

66. A Comparison of OASIS Wound Matrix With Approved Dressings for Skin Graft Donor Sites

A Comparison of OASIS Wound Matrix With Approved Dressings for Skin Graft Donor Sites A Comparison of OASIS Wound Matrix With Approved Dressings for Skin Graft Donor Sites - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save this study Warning You have reached the maximum number of saved studies (100). Please remove one or more studies before (...) adding more. A Comparison of OASIS Wound Matrix With Approved Dressings for Skin Graft Donor Sites (OASIS) The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our for details. ClinicalTrials.gov Identifier: NCT02994589 Recruitment Status : Withdrawn (Study was never started) First Posted : December 16, 2016 Last Update Posted : December 16, 2016 Sponsor

2015 Clinical Trials

67. A comparison of collagenase to hydrogel dressings in wound debridement. (Abstract)

to avoid selection bias. Subjects received daily dressing changes with either hydrogel or collagenase followed by a standard semi-occlusive dressing to evaluate time to debridement up to Day 42. Investigators, who were blinded to randomization, evaluated weekly wound photographs for necrotic tissue debridement and wound healing parameters using a digital planimetry software package. Nonviable tissue was not cross-hatched in either group.Twenty-seven nursing home residents were enrolled over a period (...) A comparison of collagenase to hydrogel dressings in wound debridement.  Comparisons of collagenase to other methods of debridement, including wet to dry dressings, have been reported in the literature; however, studies comparing collagenase to hydrogel have not been reported.Time to complete necrotic tissue debridement with collagenase compared to hydrogel in institutionalized adults with pressure ulcers.Randomization occurred after obtaining informed consent

2015 Wounds : a compendium of clinical research and practice Controlled trial quality: uncertain

68. Novel technologies can provide effective dressing and securement for peripheral arterial catheters: A pilot randomised controlled trial in the operating theatre and the intensive care unit. Full Text available with Trip Pro

Novel technologies can provide effective dressing and securement for peripheral arterial catheters: A pilot randomised controlled trial in the operating theatre and the intensive care unit. Peripheral arterial catheters are widely used in the care of intensive care patients for continuous blood pressure monitoring and blood sampling, yet failure - from dislodgement, accidental removal, and complications of phlebitis, pain, occlusion and infection - is common. While appropriate methods (...) of dressing and securement are required to reduce these complications that cause failure, few studies have been conducted in this area.To determine initial effectiveness of one dressing and two securement methods versus usual care, in minimising failure in peripheral arterial catheters. Feasibility objectives were considered successful if 90/120 patients (75%) received the study intervention and protocol correctly, and had ease and satisfaction scores for the study dressing and securement devices of ≥ 7

2015 Australian Critical Care Controlled trial quality: uncertain

69. Topical Antibiotic Ointment Versus Silver-containing Foam Dressing for Second-degree Burns in Swine. (Abstract)

Topical Antibiotic Ointment Versus Silver-containing Foam Dressing for Second-degree Burns in Swine. Second-degree burns are very common but their management is controversial. These burns may be treated with either topical antimicrobial agents or advanced occlusive dressings; however, there is no established treatment comparator for preclinical studies. This study was designed to determine which of two commonly used comparator therapies (a silver-containing advanced dressing or a topical (...) antibiotic ointment) resulted in faster reepithelialization and less scarring. The hypothesis was that second-degree burns treated with a topical antimicrobial ointment would heal faster and with less scarring than those treated with a silver-containing occlusive foam dressing in a porcine model.Deep partial-thickness burns were created on the flanks of three anesthetized female domestic pigs (20 to 25 kg) using a 150-g aluminum bar preheated in 80°C water bath and applied to the skin for 20 seconds

2015 Academic Emergency Medicine

70. Occlusive drainage system for split-thickness skin graft: A prospective randomized controlled trial. (Abstract)

: alberto.mangano@gmail.com. Marciano Laura L University Center of Statistics for the Biomedical Sciences, Vita-Salute San Raffaele University, Milan, Italy. eng Letter Comment 2017 10 09 Netherlands Burns 8913178 0305-4179 IM Burns. 2017 Mar;43(2):379-387 28341261 Burns surgery Drainage Humans Occlusive Dressings Prospective Studies Skin Transplantation 2017 05 09 2017 05 10 2017 10 17 6 0 2018 11 27 6 0 2017 10 17 6 0 ppublish 29032967 S0305-4179(17)30478-3 10.1016/j.burns.2017.05.028 (...) Occlusive drainage system for split-thickness skin graft: A prospective randomized controlled trial. 29032967 2018 11 26 2018 11 26 1879-1409 43 8 2017 12 Burns : journal of the International Society for Burn Injuries Burns Occlusive drainage system for split-thickness skin graft: A prospective randomized controlled trial. 1817 S0305-4179(17)30478-3 10.1016/j.burns.2017.05.028 Mangano Alberto A Board Certified in General Surgery, Private Practice, Lake Como, Italy. Electronic address

2018 Burns : journal of the International Society for Burn Injuries Controlled trial quality: predicted high

71. Low dose ketamine versus morphine for acute severe vaso occlusive pain in children: a randomized controlled trial. (Abstract)

Low dose ketamine versus morphine for acute severe vaso occlusive pain in children: a randomized controlled trial. Acute pain episodes associated with sickle cell disease (SCD) are very difficult to manage effectively. Opioid tolerance and side effects have been major roadblocks in our ability to provide these patients with adequate pain relief. Ketamine is cheap, widely safe, readily available drug, with analgesic effects at sub-anesthetic doses and has been used in wide range of surgeries (...) , pediatric burns dressing change and cancer related pain however, literature concerning its use in sickle cell crises is still limited in our setting. This study aimed to establish if 1 mg/kg of intravenous ketamine is non inferior to intravenous morphine 0.1 mg/kg in severe SCD-associated pain.We performed an institutional review board-approved randomized, prospective, double-blinded, active-control, non-inferiority trial at the national referral sickle cell center. Children between 7 and 18 years

2018 Scandinavian journal of pain Controlled trial quality: predicted high

72. Residual vein occlusion in relation to immediate compression and postthrombotic syndrome in deep vein thrombosis. Full Text available with Trip Pro

Residual vein occlusion in relation to immediate compression and postthrombotic syndrome in deep vein thrombosis. Thus far, the association between residual vein occlusion and immediate compression therapy and postthrombotic syndrome is undetermined. Therefore, we investigated whether compression therapy immediately after diagnosis of deep vein thrombosis affects the occurrence of residual vein obstruction (RVO), and whether the presence of RVO is associated with postthrombotic syndrome (...) and recurrent venous thromboembolism. In a prespecified substudy within the IDEAL (individualized duration of elastic compression therapy against long-term duration of therapy for prevention of postthrombotic syndrome) deep vein thrombosis (DVT) study, 592 adult patients from 10 academic and nonacademic centers across The Netherlands, with objectively confirmed proximal DVT of the leg, received no compression or acute compression within 24 hours of diagnosis of DVT with either multilayer bandaging

2018 Blood Controlled trial quality: uncertain

73. Medihoney dressing (Derma Sciences Inc.) for wound healing

to Australia and New Zealand. Honey can be applied directly to the wound bed, or on gauze dressing and placed over the wound, or a commercially available product can be used. Final publication URL The report may be purchased from: Indexing Status Subject indexing assigned by CRD MeSH Honeys; Occlusive Dressings; Wound Healing Language Published English Country of organisation United States English summary An English language summary is available. Address for correspondence HAYES, Inc., 157 S. Broad Street (...) Medihoney dressing (Derma Sciences Inc.) for wound healing Medihoney dressing (Derma Sciences Inc.) for wound healing Medihoney dressing (Derma Sciences Inc.) for wound healing Record Status This is a bibliographic record of a published health technology assessment. No evaluation of the quality of this assessment has been made for the HTA database. Citation Medihoney dressing (Derma Sciences Inc.) for wound healing. Lansdale: HAYES, Inc.. Healthcare Technology Brief Publication. 2010 Authors

2010 Health Technology Assessment (HTA) Database.

74. Prevention of Radial Artery Occlusion After Transradial Access Using Nitroglycerin

Prevention of Radial Artery Occlusion After Transradial Access Using Nitroglycerin Prevention of Radial Artery Occlusion After Transradial Access Using Nitroglycerin - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save this study Warning You have reached the maximum number of saved studies (100). Please remove one or more studies before (...) adding more. Prevention of Radial Artery Occlusion After Transradial Access Using Nitroglycerin (Patens) The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. of clinical studies and talk to your health care provider before participating. Read our for details. ClinicalTrials.gov Identifier: NCT03158532 Recruitment Status : Recruiting First Posted : May 18, 2017

2017 Clinical Trials

75. Evaluation of Efficacy, Duration of Remission and Safety of a Light and Occlusive Patch Therapy for Plaque Psoriasis

. ClinicalTrials.gov Identifier: NCT03180866 Recruitment Status : Recruiting First Posted : June 8, 2017 Last Update Posted : June 8, 2017 See Sponsor: Illumicure Inc Information provided by (Responsible Party): Illumicure Inc Study Details Study Description Go to Brief Summary: This is a proof of concept, investigator blinded study to evaluate the efficacy and safety of a novel combination of a home narrow band ultraviolet B (NBUVB) lamp with an occlusive dressing in adult subjects with mild to moderate psoriasis (...) vulgaris. Two interpatient arms will be used to compare the efficacy of combination of NBUVB with an occlusive dressing (active) to no treatment (control). 32 patients will be enrolled in this 30 week study. Condition or disease Intervention/treatment Phase Psoriasis Device: Luma Light System Not Applicable Detailed Description: This is a multi-center, investigator blinded, randomized study designed to assess the efficacy, duration of effect, safety and tolerability of Luma Light System for plaque

2017 Clinical Trials

76. Occlusive drainage system for split-thickness skin graft: A prospective randomized controlled trial. (Abstract)

Occlusive drainage system for split-thickness skin graft: A prospective randomized controlled trial. Split-thickness skin grafts are widely used in reconstruction of large area defects. Conventional postoperative recipient site care includes saline-moistened gauze with a protective layer of petroleum gauze and splints for immobilization. This method causes pain while changing the dressing. We designed a better occlusive drainage system for split-thickness skin grafts. We compared the treatment (...) effect and subjective evaluation of our occlusive drainage system with that of the conventional method for coverage of split-thickness skin grafts.A randomized controlled trial was carried out in patients who received split-thickness skin grafts. Patients aged 24-76 years were randomly assigned to the occlusive drainage system or the conventional indirect wet dressing method. The status of graft take, pain, and subjective evaluations were compared.Twenty-eight participants were enrolled, with 14

2017 Burns : journal of the International Society for Burn Injuries Controlled trial quality: uncertain

77. Use of Banana Leaf Dressing on Donor Site Wounds

for autoclaving. The Banana Leaf Dressing site will receive a single layer of banana leaf without any topical antibiotic applied to the wound followed by a layer of dry gauze for absorption of exudates. The dressing is secured with cling wrap to maintain an occlusive environment. This is then covered by rolled gauze and elastic bandage. Active Comparator: Hydrocolloid Dressing Arm The donor under Hydrocolloid dressing was covered with hydrocolloid (DuoDERM CGF). Drug: Hydrocolloid Dressing (DuoDERM CGF (...) ) The donor under HCD was covered with hydrocolloid (DuoDERM CGF). The hydrocolloid dressing was cut to the size of the donor site with an overlap of at least 2 centimeter around the wound edge. After pulling off the adhesive backing, care was taken to ensure that the adhesive was in direct contact with the raw surface. This was likewise covered with a top dressing of gauze for absorption of exudates and an elastic bandage to secure dressing. Outcome Measures Go to Primary Outcome Measures : Healing

2014 Clinical Trials

78. Topical petrolatum gel alone versus topical silver sulfadiazine with standard gauze dressings for the treatment of superficial partial thickness burns in adults: A randomized controlled trial. (Abstract)

to support or refute such antimicrobial prophylaxis. Another review compared silver sulfadiazine dressings with other occlusive and non-antimicrobial dressings and found insufficient evidence to guide practice. Other research has suggested that dressings with petrolatum gel are as effective as silver sulfadiazine.Single-center, randomized, controlled parallel group trial comparing conventional silver sulfadiazine dressings with treatment with petrolatum gel alone. Consenting adults 18-45 years old (...) Topical petrolatum gel alone versus topical silver sulfadiazine with standard gauze dressings for the treatment of superficial partial thickness burns in adults: A randomized controlled trial. Non-extensive superficial partial thickness burns constitute a major proportion of burns. Conventional treatment involves regular changing of absorptive dressings including the application of a topical antimicrobial, commonly silver sulfadiazine. A systematic review has found insufficient evidence

2014 Burns : journal of the International Society for Burn Injuries Controlled trial quality: uncertain

79. "Pocket sandwich" dressing in auricular surgery. (Abstract)

"Pocket sandwich" dressing in auricular surgery. The auricular dressing presents a challenge to medical staff and patients alike. The task is to dress the ear, which may include exposed cartilage, in a manner that provides protection but does not distort auricular anatomy.Two lengths of adhesive tape are sandwiched over the posterior and anterior aspects of the ear to cover the defect in an occlusive manner, creating a "pocket sandwich"-type dressing.This method results in a dressing that can (...) be used to cover a post-surgical defect on any part of the ear. It is inexpensive and easily reproducible by the patient.The present dressing is non-bulky, easy to perform, and encases the ear in a pocket of adhesive tape. Further advantages are that it avoids the auricular distortion that may occur with overly bulky dressings, provides an occlusive environment, is esthetically pleasing, and comfortably accommodates eyewear. We highly recommend its use for ear wound defects.© 2014 The International

2014 International Journal of Dermatology

80. A Preliminary Study of Silver Sodium Zirconium Phosphate Polyurethane Foam Wound Dressing on Wounds of the Distal Aspect of the Forelimb in Horses. (Abstract)

A Preliminary Study of Silver Sodium Zirconium Phosphate Polyurethane Foam Wound Dressing on Wounds of the Distal Aspect of the Forelimb in Horses. To determine if application of silver sodium zirconium phosphate polyurethane semi-occlusive foam (SPF) dressing would improve measures of wound healing and decrease bacterial contamination compared with a non-adherent, absorbent dressing applied to wounds created on the distal aspect of the equine limb.Controlled randomized experimental study.Adult (...) Quarter Horse and Thoroughbred horses (n = 5).One 6.25 cm(2) wound was created on the dorsomedial aspect of the proximal metacarpus on each forelimb. A SPF dressing was applied to 1 randomly assigned limb as a treatment and a non-adherent, absorbent dressing was applied to the opposite limb as control. Bandages were changed every 3 days for 60 days. Granulation tissue was scored every 3 days, wound area measured every 6 days, and wound bed was cultured every 12 days.SPF-treatment wounds had

2014 Veterinary surgery : VS Controlled trial quality: uncertain

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