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Laser Skin Procedure

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81. A Study Using Fractional Carbon Dioxide and Long Pulsed Neodymium-yttrium Aluminum Garnet Lasers in Treatment of Keloids

form of treatment during the last four weeks prior to treatment such as intralesional steroids or a laser procedure during the last six months. Patients with active skin infections e.g. herpes or autoimmune disease. Patients with previous history of adverse outcome related to laser therapy. Recent use of Isotretinoin (within 6 months prior to the procedure). Patients with known allergies to lidocaine. Smoking, pregnancy Patients with unrealistic expectations Contacts and Locations Go to Information (...) A Study Using Fractional Carbon Dioxide and Long Pulsed Neodymium-yttrium Aluminum Garnet Lasers in Treatment of Keloids A Study Using Fractional Carbon Dioxide and Long Pulsed Neodymium-yttrium Aluminum Garnet Lasers in Treatment of Keloids - 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

2018 Clinical Trials

82. Confocal Laser Endomicroscopy With Topical Cresyl Violet for Colorectal Polyps

: August 8, 2018 See Sponsor: Shandong University Information provided by (Responsible Party): Yanqing Li, Shandong University Study Details Study Description Go to Brief Summary: Probe-based confocal laser endomicroscopy (pCLE) has been shown to a reliable diagnostic method enabling in vivo microscopic imaging during ongoing endoscopy. Usually fluorescein then serves as a contrast agent for pCLE, but it does not allow direct nuclear visualization, must be injected, leads to a transient skin (...) Confocal Laser Endomicroscopy With Topical Cresyl Violet for Colorectal Polyps Confocal Laser Endomicroscopy With Topical Cresyl Violet for Colorectal Polyps - 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

2018 Clinical Trials

83. Laser Therapy for Vulvovaginal Symptoms in Breast Cancer Patients

Product: No Studies a U.S. FDA-regulated Device Product: No Keywords provided by Royal North Shore Hospital: genitourinary symptoms of menopause CO2 fractional ablative laser Early breast cancer Vulvovaginal atrophy Vaginal dryness Dyspareunia Vaginal itch Dysuria Additional relevant MeSH terms: Layout table for MeSH terms Breast Neoplasms Atrophy Neoplasms by Site Neoplasms Breast Diseases Skin Diseases Pathological Conditions, Anatomical (...) Laser Therapy for Vulvovaginal Symptoms in Breast Cancer Patients Laser Therapy for Vulvovaginal Symptoms in Breast Cancer 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. Laser Therapy

2018 Clinical Trials

84. Clinical Evaluation of the Safety and Efficacy of a 1060nm Diode Laser (Abdomen)

provided by the sponsor. Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03756350 Locations Layout table for location information United States, California Laser and Skin Surgery Center of Northern California Sacramento, California, United States, 95816 United States, Texas Southwestern Medical Center Department of Plastic Surgery Dallas, Texas, United States, 75390 Sponsors and Collaborators Venus Concept Investigators Layout table for investigator information Study (...) Director: Tracey Lizsa Mancuso Venus Concept Principal Investigator: Suzanne Kilmer, MD Skin and Laser Surgery Center of Northern California Principal Investigator: Jeffery Kenkel, MD UT Southwestern More Information Go to Publications of Results: Layout table for additonal information Responsible Party: Venus Concept ClinicalTrials.gov Identifier: Other Study ID Numbers: CS1317 First Posted: November 28, 2018 Last Update Posted: February 28, 2019 Last Verified: February 2019 Individual Participant

2018 Clinical Trials

85. Clinical Evaluation of the Safety and Efficacy of a 1060 nm Diode Laser (Flanks)

table for location information United States, California Laser and Skin Surgery Center of Northern California Sacramento, California, United States, 95816 United States, Texas UT Southwestern Medical Centre Dallas, Texas, United States, 75390 Sponsors and Collaborators Venus Concept Investigators Layout table for investigator information Study Director: Tracey Lizsa Mancuso Venus Concept Principal Investigator: Suzanne Kilmer, MD Skin and Laser Centre of Northern California Principal Investigator (...) Clinical Evaluation of the Safety and Efficacy of a 1060 nm Diode Laser (Flanks) Clinical Evaluation of the Safety and Efficacy of a 1060 nm Diode Laser (Flanks) - 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

2018 Clinical Trials

86. Transcanalicular laser dacryocystorhinostomy for acquired nasolacrimal duct obstruction: an audit of 104 patients Full Text available with Trip Pro

Transcanalicular laser dacryocystorhinostomy for acquired nasolacrimal duct obstruction: an audit of 104 patients External dacryocystorhinostomy (DCR) is considered as the gold standard in the treatment of acquired nasolacrimal duct obstruction. However, many advances have been made towards the development of modern minimally invasive therapies. These new techniques were proven less harmful to the patients' skin and medial palpebral structures with their palpebral-canalicular pump mechanism (...) . Options include endonasal and transcanalicular procedures. Here, we report on our 2-year experience with the surgical technique, results and complications of transcanalicular laser-assisted DCR.This is a retrospective study. A total of 104 patients with acquired nasolacrimal duct obstruction underwent transcanalicular laser-assisted DCR combined with bicanalicular silicon intubation. We then analyzed intra-/post-operative complications and subjective and objective success rates. The institutional

2018 European Journal Of Medical Research

87. Post-Surgical Repair of Cleft Scar Using Fractional CO2 Laser Full Text available with Trip Pro

, pliability, thickness & colour of the skin and Visual Analogue Scale VAS from (0-10) was used to assess the severity of pain as well as a survey questionnaire for the rate of patient's satisfaction. Also, digital clinical photos assessment before&after were compared.Patients expressed a significantly greater degree of satisfaction with the treatment using a subjective 4-point scale. All patients observed dramatic improvement in their lip scars after FCO2 laser sessions following their surgeries (...) Post-Surgical Repair of Cleft Scar Using Fractional CO2 Laser Postoperative scarring is a common cause of patients dissatisfaction. Several modalities have been developed to overcome such a problem following surgical repair. Despite precise surgical technique, still, some scars would remain over the time, mostly due to the weak formation or inadequately replaced collagen fibres in the underneath dermis especially those following unilateral or bilateral cleft lip repair surgery.of this study

2018 Open access Macedonian journal of medical sciences

88. Open-label, Prospective, Multicenter Study to Evaluate the Cutera Excel Vâ„¢ Laser and a Micro-Lens Array Attachment

treatment to the target area within 6 months of study participation, such as laser procedures, facial fillers, toxins and those used for general aesthetic correction. Use of prescription topicals in the treatment area within one month prior to treatment or use of topical agents one week prior to treatment that may cause facial sensitivity. Suffering from significant skin conditions in the treated areas or inflammatory skin conditions, including but not limited to, open lacerations or abrasions (...) . ClinicalTrials.gov Identifier: NCT03424148 Recruitment Status : Recruiting First Posted : February 6, 2018 Last Update Posted : March 15, 2018 See Sponsor: Cutera Inc. Information provided by (Responsible Party): Cutera Inc. Study Details Study Description Go to Brief Summary: Open-label, Prospective, Study to Evaluate the Cutera excel V laser at 532 nm in a low fluence, high repetition rate mode and the Micro-Lens Array attachment used with excel V laser at 1064 nm and 532 nm for the improvement of skin quality

2018 Clinical Trials

89. Evaluation of the Cutera Enlightenâ„¢ Laser With Micro-Lens Array (MLA) Handpiece Attachment

6 months of study participation, such as laser procedures, facial fillers, i.e. (Bellafill) and those used for general aesthetic correction, facial peel, lightening creams, or facial surgery. Use of prescription topicals in the treatment area within one month prior to treatment or use of topical agents one week prior to treatment that may cause facial sensitivity. Suffering from significant skin conditions in the treated areas or inflammatory skin conditions, including but not limited to, open (...) and sign the Informed Consent Form. Female or Male, 18 to 65 years of age (inclusive). Fitzpatrick Skin Type I - VI (Appendix 6). Subject desires treatment for acne scars and wishes to undergo laser treatments for improvement. Subject has bilateral moderate to severe signs of facial acne scarring. Must be willing to have Cutera enlighten laser with the Micro-Lens Array handpiece attachment treatments and able to adhere to the treatments, follow-up visit schedule, and post-treatment care instructions

2018 Clinical Trials

90. Aerobic Exercise and Transcranial Low Laser Therapy in Patients With Central Nervous System Injury

equipment (BrainMov® Physical Activity Station). The transcranial photobiomodulation (laser diode, λ = 810 nm, beam area 0.028 cm², power of 100 mW, power density of 3.5 mW / cm², energy of 3 Joules / point and energy density of 107.1 J / cm2) will be applied on the skin / scalp and the International System 10-20 at points F7, F8 and AFz will be used as reference for irradiation. Muscular activation, heart rate variability, lung volumes and capacities, fatigability, exercise tolerance, cognition (...) Estimated Primary Completion Date : July 31, 2019 Estimated Study Completion Date : March 5, 2020 Resource links provided by the National Library of Medicine related topics: Arms and Interventions Go to Arm Intervention/treatment Active Comparator: Control-Cardiorespiratory Rehabilitation These individuals will compose the control group for transcranial laser therapy, which will only receive cardiorespiratory rehabilitation. Procedure: Cardiorespiratory Rehabilitation Cardiorespiratory Rehabilitation

2018 Clinical Trials

91. Randomized Trial :Hemorrhoidal Pedicle Ligation vs Laser vs Open Hemorrhoidectomy

Intrahaemoroidal laser coagulation Intrahaemoroidal laser coagulation is performed using disposable THD kit [Biolitec Co]. The haemorrhoidal pedicle is sutured. 1mm opening is created at the external haemorrhoid (skin level). Laser is then introduced up to pedicle and coagulation performed. This is repeated to all the piles. The procedure is finished with placing Spongostan plug into anal canal Procedure: Haemorrhoidectomy operations for treatment of symptomatic 2 to 3 degree haemorrhoids Outcome Measures Go (...) Collaborator: Biolitec Pharma Ltd. Information provided by (Responsible Party): Tomas Poskus, Vilnius University Study Details Study Description Go to Brief Summary: The aim of this study is to compare three different modalities for treatment of symptomatic 2 ° to 3 ° haemorrhoids: open haemorrhoidectomy, intrahaemorrhoidal laser procedure and haemorrhoidal pedicle ligation. To assess early outcomes (after one week and one month) of the procedures: pain, bleeding, wound healing, return to work and quality

2018 Clinical Trials

92. Objective analysis of volume restoration in atrophic acne scars and skin pores: A split study using human stem cell-conditioned media. (Abstract)

Objective analysis of volume restoration in atrophic acne scars and skin pores: A split study using human stem cell-conditioned media. Background: It is anticipated that the combined treatments of ablative laser and human stem cell-conditioned media produce the synergistic effects. Objectives: To investigated the effects of human stem cell-conditioned media (HSCM) as a post-procedural agent after fractional CO2 laser procedure in patients with atrophic acne scars and skin pores. Method: Both (...) ) versus 15.0% (C) (p = .143) and the volume of the skin pores was reduced by 37.6% (T) versus 15.9% (C) (p = .006), while the erythema was increased by 2.8% (T) versus 3.1% (C) (p = .934). Atrophic scar and the skin pores in the HSCM-applied area improved by at least 15.0% after a single treatment session, suggesting better results compared with the control side. Conclusion: HSCM may augment the regenerative effects of fractional CO2 laser.

2019 Journal of Dermatological Treatment Controlled trial quality: uncertain

93. Can Fractionated Microneedle Radiofrequency be an Effective Procedure for Treatment of Fox–Fordyce Disease? A Medical Hypothesis Full Text available with Trip Pro

Can Fractionated Microneedle Radiofrequency be an Effective Procedure for Treatment of Fox–Fordyce Disease? A Medical Hypothesis 29862220 2018 11 14 2277-9175 7 2018 Advanced biomedical research Adv Biomed Res Can Fractionated Microneedle Radiofrequency be an Effective Procedure for Treatment of Fox-Fordyce Disease? A Medical Hypothesis. 71 10.4103/abr.abr_288_16 Kabiri Sattar S Department of Orthodontic, Dental School, Shahid Beheshti University of Medical Sciences, Tehran, Iran. Pourazizi (...) Mohsen M Cancer Research Center, Semnan University of Medical Sciences, Semnan, Iran. Abtahi-Naeini Bahareh B Skin Diseases and Leishmaniasis Research Center, Department of Dermatology, Isfahan University of Medical Sciences, Isfahan, Iran. eng Journal Article 2018 04 24 India Adv Biomed Res 101586897 2277-9175 There are no conflicts of interest. 2018 6 5 6 0 2018 6 5 6 0 2018 6 5 6 1 epublish 29862220 10.4103/abr.abr_288_16 ABR-7-71 PMC5952534 J Drugs Dermatol. 2009 Mar;8(3):259-65 19271373 J Am

2018 Advanced biomedical research

94. Accuvein Versus Standard Care for Intravenous Cannulation Procedure in Children

the visualization of veins and thus the insertion of cannulation. The AccuVein®400 (AV400) system uses an infrared laser beam to project the image of superficial veins to the skin. In adults, AV400 has been shown to improve the success rate of insertion cannulation when venous capital is precarious. The question now arises as to whether this tool could be of interest to children who are particularly difficult to assist cannulation, especially the youngest of them. Investigator hypothesize that AV400 could bring (...) for peripheral intravenous cannulation Experimental: Accuvein system uses an infrared laser beam to project the image of superficial veins to the skin Device: Accuvein®400 The intervention comes down to the randomization of the standard treatment versus Accuvein for peripheral intravenous cannulation Outcome Measures Go to Primary Outcome Measures : successful of cannulation at first attempt [ Time Frame: At day 1 (at the moment of peripheral intravenous cannulation) ] Percentage of children whose peripheral

2018 Clinical Trials

95. Skin Cancer Treatment (PDQ®): Health Professional Version

do not become SCCs. These typically red, scaly patches usually arise on areas of chronically sun-exposed skin and are likely to be found on the face and dorsal aspects of the hand. Diagnostic and Staging Evaluation BCC and SCC are usually diagnosed on the basis of routine histopathology obtained from a shave, punch, incisional, or excisional biopsy.[ ] Other tests and procedures may be incorporated into the diagnosis and staging of BCC and SCC of the skin when appropriate and include (...) Squamous cell carcinoma Localized disease Metastatic or locally advanced disease untreatable by local modalities Recurrent nonmetastatic disease Actinic keratosis Localized disease Basal Cell Carcinoma of the Skin Treatment There is a wide range of approaches for treating basal cell carcinoma (BCC) of the skin, including excision, radiation therapy, cryosurgery, electrodesiccation and curettage, photodynamic or laser-beam light exposure, and topical therapies. Each of these approaches is useful

2017 PDQ - NCI's Comprehensive Cancer Database

96. Laser Induced Bioengineered Remodeling of Thermally Injured Skin Trial

Laser Induced Bioengineered Remodeling of Thermally Injured Skin Trial Laser Induced Bioengineered Remodeling of Thermally Injured Skin Trial - 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. Laser Induced (...) Carolina, Chapel Hill Information provided by (Responsible Party): University of North Carolina, Chapel Hill Study Details Study Description Go to Brief Summary: This study will evaluate the efficacy of pulsed dye laser (PDL) and carbon dioxide (CO2) laser in conjunction with usual care (MED) for the treatment of hypertrophic burn scars and will determine the optimal sequence and timing of lasers and usual care. Condition or disease Intervention/treatment Phase Hypertrophic Scars Procedure: CO2 laser

2014 Clinical Trials

97. Laser-skinning colpectomy for extended vaginal intraepithelial neoplasia and microinvasive cancer. Full Text available with Trip Pro

was lost. Of 23 patients with follow-up ≥12months, 20 were disease free after a single laser-skinning colpectomy (overall cure rate 87.0%). Moderate shortening of the vagina was observed in two patients and another two required reconstruction of vaginal strictures during long-term follow-up.Laser-skinning colpectomy appears to be a feasible treatment for extended high-risk VaIN3. The procedure avoids the mutilation associated with colpectomy and allows early diagnosis and staging of invasive (...) Laser-skinning colpectomy for extended vaginal intraepithelial neoplasia and microinvasive cancer. The aim of this study is to analyze the efficacy of colposcopic-guided laser-skinning colpectomy to treat extended high-grade vaginal intraepithelial neoplasia (VaIN).Retrospective review of 33 heavily pretreated patients with high-grade VaIN extending over 20-100% of the vaginal surface treated between 2003 and 2013 with colposcopic-guided laser-skinning colpectomy. The vaginal epithelium

2014 Gynecologic Oncology

98. Closure of Skin Incision Using CO2 Laser

Closure of Skin Incision Using CO2 Laser Closure of Skin Incision Using CO2 Laser - 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. Closure of Skin Incision Using CO2 Laser The safety and scientific validity (...) is to evaluate the safety and effectiveness of using Temperature Controlled Laser Soldering System for soft tissue bonding. Condition or disease Intervention/treatment Phase Wound Device: Temperature Controlled Laser Soldering Phase 1 Detailed Description: Skin incisions can be closed by a variety of method which create temporary approximation of the wound edges until natural healing process ensue and reach a phase, where it is closed and can sustain the daily tensile forces. The wound closure devices

2014 Clinical Trials

99. Fractional Carbon Dioxide Laser Treatment to Enhance Skin Permeation of Ascorbic Acid 2-Glucoside with Minimal Skin Disruption. (Abstract)

Fractional Carbon Dioxide Laser Treatment to Enhance Skin Permeation of Ascorbic Acid 2-Glucoside with Minimal Skin Disruption. Topical treatment with vitamin C has been used to treat photoaged skin and as a skin whitener, but no standard procedure exists for percutaneous delivery.To compare skin histology and the permeation of ascorbic acid 2-glucoside (AA2G) after fractional and conventional carbon dioxide (CO(2) ) laser pretreatment.The effect on porcine skin of treatment with different (...) strengths of fractional and conventional CO(2) laser treatment was examined using scanning electron microscopy and transmission electron microscopy. Permeation of AA2G through porcine skin was tested in vitro using a Franz diffusion chamber. In vivo changes in fluorescein thiocyanate permeability in nude mice were examined using confocal laser scanning microscopy.Fractional CO(2) laser treatment with four or fewer passes caused less disruption than conventional laser treatment at the same fluence

2012 Dermatologic Surgery

100. Pain in Naïve and Non-naïve Subjects Undergoing Nonablative Skin Tightening Dermatologic Procedures: A Nested Randomized Control Trial. (Abstract)

Pain in Naïve and Non-naïve Subjects Undergoing Nonablative Skin Tightening Dermatologic Procedures: A Nested Randomized Control Trial. Pain is expected during noninvasive skin tightening and can be anxiety provoking, especially for those who have not had prior treatments.To compare pain reported by patients naïve to nonablative skin tightening energy devices with those who were not naive.The non-naïve group at least three nonablative laser procedures or one nonablative skin tightening (...) procedure, and the naïve group no previous treatments. Four sites at each of two anatomic locations (periorbital and midface or cheek) were treated in each subject with needle prick, pulsed dye laser, radiofrequency, and ultrasound with the order of the interventions randomized. All interventions except ultrasound were also applied to three abdominal sites. The difference in mean pain scores between naïve and nonnaïve subjects were averaged over the anatomic sites.Ten naïve and 10 non-naïve subjects

2014 Dermatologic Surgery Controlled trial quality: uncertain

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