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Laser Skin Procedure

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161. Randomized Clinical Trial Evaluating the Use of the Laser-Assisted Immunotherapy (LIT/inCVAX) in Advanced Breast Cancer

Randomized Clinical Trial Evaluating the Use of the Laser-Assisted Immunotherapy (LIT/inCVAX) in Advanced Breast Cancer Randomized Clinical Trial Evaluating the Use of the Laser-Assisted Immunotherapy (LIT/inCVAX) in Advanced Breast Cancer - 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. Randomized Clinical Trial Evaluating the Use of the Laser-Assisted Immunotherapy (LIT/inCVAX) in Advanced Breast Cancer 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: NCT03202446 Recruitment Status : Terminated First

2017 Clinical Trials

162. The Effect of Fractional Co2 Laser Either With Tacrolimus, Calcipotriol or NB-UVB in Stable Generalized Vitiligo

for skin resurfacing based on the theory of fractional photothermolysis introduced by Manstein et al (2004). These lasers were shown to be efficient in treating facial photo aging changes as well as scars, and have an improved safety and recovery profile compared with traditional CO2 laser resurfacing. Fractionated lasers do not ablate the entire epidermis and thereafter leave intact skin between coagulated necrotic columns. This characteristic facilitates the skin healing process (Bogdan et al., 2010 (...) The Effect of Fractional Co2 Laser Either With Tacrolimus, Calcipotriol or NB-UVB in Stable Generalized Vitiligo The Effect of Fractional Co2 Laser Either With Tacrolimus, Calcipotriol or NB-UVB in Stable Generalized Vitiligo - 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

2017 Clinical Trials

163. Advanced film-forming gel formula vs spring thermal water and white petrolatum as primary dressings after full face ablative fractional CO2 laser resurfacing: A comparative split-face pilot study. (Abstract)

-blinded, prospective observational study was to assess the efficacy and acceptability of two primary wound dressings immediately after a full-face fractional CO2 laser resurfacing procedure.The assessments of an innovative film-forming dressing called Stratacel (SC) vs spring thermal water + Vaseline (V+) were conducted after a standardized, single-pass, full-face ablative fractional CO2 laser skin resurfacing procedure. Clinical parameters, such as haemoglobin - HB; surface temperature - ST; micro (...) Advanced film-forming gel formula vs spring thermal water and white petrolatum as primary dressings after full face ablative fractional CO2 laser resurfacing: A comparative split-face pilot study. Aesthetically pleasing results and fast, uneventful recovery are highly desirable after rejuvenating ablative laser procedures. Wound dressings following ablative laser procedures should ideally improve and optimize the wound healing environment.The purpose of this comparative split-face, single

2017 Journal of the European Academy of Dermatology and Venereology

164. The Effects of Transcutaneous and Intraoral Low-Level Laser Therapy After Extraction of Lower Third Molars: A Randomized Single Blind, Placebo Controlled Dual-Center Study. (Abstract)

The Effects of Transcutaneous and Intraoral Low-Level Laser Therapy After Extraction of Lower Third Molars: A Randomized Single Blind, Placebo Controlled Dual-Center Study. The surgical removal of impacted third molars is one of the most common procedures performed by oral and maxillofacial surgeons. The purpose of this study is to determine whether either transcutaneous or intraoral low-level laser therapy (LLLT) reduces postoperative pain and assists in the healing of mandibular third molar (...) extraction.This randomized, placebo controlled, single-blind, split-mouth design study was conducted on 60 patients with full bony impacted similar position mandibular third molars bilaterally. The patients were divided into two groups of 30 each: transcutaneous LLLT and intraoral LLLT and the other side of each group treated with nonactive laser (60 teeth). The laser treatment consisted of administering laser energy immediately before and after the extraction procedure with gallium aluminum arsenide (GaAlAs

2017 Photomedicine and laser surgery Controlled trial quality: uncertain

165. Safety and Efficacy Evaluation of Pulsed Dye Laser Treatment, CO<sub>2</sub> Ablative Fractional Resurfacing, and Combined Treatment for Surgical Scar Clearance. (Abstract)

Safety and Efficacy Evaluation of Pulsed Dye Laser Treatment, CO2 Ablative Fractional Resurfacing, and Combined Treatment for Surgical Scar Clearance. Surgical scars are an unwanted sequela following surgical procedures. Several different treatment modalities and approaches are currently being employed to improve the cosmesis of surgical scars with each having varying degrees of success. The objective of this study was to assess the ef cacy and safety pulsed dye laser treatment, CO2 (...) ablative fractional resurfacing, and a combined treatment with these two modalities for the cosmetic improvement of surgical scarring that occurred following the surgical removal of skin cancer from different anatomic areas.Twenty-five patients with surgical scarring most frequently on the face following recent surgical excision of skin cancer with Mohs surgery were included in this multicenter, prospective clinical study. Patients were randomized into 4 treatment arms, namely, pulsed dye laser alone

2017 Journal of drugs in dermatology : JDD Controlled trial quality: uncertain

166. A retrospective review of light- and laser-based management of hidradenitis suppurativa. (Abstract)

A retrospective review of light- and laser-based management of hidradenitis suppurativa. Hidradenitis suppurativa (HS) is a chronic skin disease that is difficult to manage and often refractory to medical management. Light and laser therapies have been utilized in the field of dermatology to treat a variety of skin conditions, but more recently were studied in the management of HS. Usually performed as outpatient procedures with a low risk of complications, they offer several advantages (...) to traditional cold knife surgical procedures. We reviewed the various light- and laser-based treatments studied in HS and compared their efficacy. Outcome measures were not standardized, which made comparison difficult. Studies performed were few in number and often limited by small patient samples. Larger, randomized controlled trials that compare these treatment modalities to medical and surgical management are needed. Despite their limitations, light- and laser-based therapies are promising treatment

2017 Seminars in Cutaneous Medicine and Surgery

167. Surgical Scar Treatment With the Pulsed Dye Laser in Combination With a CO2 Laser

Adult) Sexes Eligible for Study: All Accepts Healthy Volunteers: Yes Criteria Inclusion Criteria: Comprehension of, and willingness to sign, the Informed Consent Form. Have a planned a surgical procedure, which is expected to result in a least one linear surgical scar of at least 3.0 cm. Be a healthy male or female of at least 18 years old. Fitzpatrick skin type I-V. Willingness to follow the treatment and follow-up schedule and the post-treatment care instructions. Non pregnant and/or breast (...) feeding, if applicable. Willingness to provide a brief medical history including disclosure of any prescribed or over-the-counter medications taken within the past 6 months. Agree to follow and undergo all study-related procedures. Use of daily use of sunblock SPF 30 or higher for duration of the study. Exclusion Criteria: Pregnant and/or breastfeeding. Fitzpatrick skin type VI. Prior treatment for the surgical scar to be treated in this study. Having a history of diseases stimulated by heat

2016 Clinical Trials

168. Effect of Procedural-Related Variables on Melanocyte-Keratinocyte Suspension Transplantation in Nonsegmental Stable Vitiligo: A Clinical and Immunocytochemical Study. (Abstract)

with nonsegmental stable vitiligo. Donor site was either a skin graft in noncultured epidermal cell suspension (NCECS) or hair follicle units in outer root sheath hair follicle suspension (ORSHFS). Recipient site was prepared by either cryoblebbing or CO2 laser resurfacing. Cell counts and viability were recorded in the cell suspensions. Tissue melanocytes and keratinocytes were examined by melan-A and cytokeratin, respectively. Assessment of repigmentation was performed 18 months after the procedure.Thirty (...) Effect of Procedural-Related Variables on Melanocyte-Keratinocyte Suspension Transplantation in Nonsegmental Stable Vitiligo: A Clinical and Immunocytochemical Study. Melanocyte-keratinocyte suspension (M-K susp) is gaining popularity for vitiligo treatment. Few studies have addressed procedure-related variables.To assess the effect of different M-K susp procedure-related variables on the clinical outcome in stable vitiligo.This prospective multicenter comparative study included 40 cases

2017 Dermatologic Surgery

169. Efficacy of Long Pulsed 1064nm Laser for Facial Skin Tightening

Efficacy of Long Pulsed 1064nm Laser for Facial Skin Tightening Efficacy of Long Pulsed 1064nm Laser for Facial Skin Tightening - 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. Efficacy of Long Pulsed 1064nm (...) Laser for Facial Skin Tightening 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: NCT01971736 Recruitment Status : Completed First Posted : October 29, 2013 Last Update Posted : October 29, 2013 Sponsor: Phramongkutklao College of Medicine and Hospital Information provided by (Responsible Party

2013 Clinical Trials

170. Single Treatment with 100-Microsecond Alexandrite Laser Clears Selected Acquired Melanocytic Nevi in Type IV Asian Facial Skin Full Text available with Trip Pro

Single Treatment with 100-Microsecond Alexandrite Laser Clears Selected Acquired Melanocytic Nevi in Type IV Asian Facial Skin Small common acquired melanocytic nevi (AMNs) are common on Asian facial skin.To show that the 755 nm Alexandrite laser stacked at the 100-μs long-pulsed mode (μsAL) is an effective modality for the removal of selected AMNs.This was a retrospective case series, followed up with a telephone interview.A retrospective analysis of all patients treated between January 2010 (...) and April 2012 with the μsAL laser for small AMNs was conducted. Pre- and post-treatment facial photographs and photographs of the individual lesions were analyzed by two independent dermatological surgeons for degree of clearance and complications. A telephone interview was conducted with the patients to assess their satisfaction with the procedure.A total of 18 patients with 53 lesions were included. 7/18 (38.9%) of patients had 'excellent' results. No patients had 'mild' or 'poor' results. At 4 week

2013 Journal of cutaneous and aesthetic surgery

171. Facial skin and soft tissue infection caused by Mycobacterium wolinskyi associated with cosmetic procedures. Full Text available with Trip Pro

(200 mg every 8 h), and ciprofloxacin (400 mg every 6 h).We report the first case of facial skin and soft tissue infection with M. wolinskyi after multiple cosmetic procedures of filler injection and laser lipolysis. Increased occurrence of NTM infection in nosocomial settings suggests the importance of appropriate treatment including culturing and rpoB gene sequencing when patients who have undergone cosmetic procedures display symptoms and signs of soft tissue infection indicative of NTM (...) Facial skin and soft tissue infection caused by Mycobacterium wolinskyi associated with cosmetic procedures. Mycobacteirum wolinskyi is a member of the Mycobacterium smegmatis group, which is less frequently found in clinical settings than other nontuberculous mycobacterium (NTM) species. However, its clinical significance has recently increased in opportunistic infections. This case is the first report of facial skin and soft tissue infection by M. wolinskyi complicating cosmetic procedures.A

2013 BMC Infectious Diseases

172. Comparative Study of Diode Laser Versus Neodymium-Yttrium Aluminum: Garnet Laser Versus Intense Pulsed Light for the Treatment of Hirsutism Full Text available with Trip Pro

. The percentage of hair reduction after eight sessions of treatment was maximum (92%) in the diode laser group, followed by 90% hair reduction in the Nd: YAG group and 70% hair reduction in the IPL group.To conclude for the Indian skin with dark hairs, the diode laser still stands the test of time. But, since the diode laser has a narrow margin of safety, proper pre and post-procedure cooling is recommended. Although, the side effects of Nd: YAG laser are less as compared to the diode laser, it is less (...) Comparative Study of Diode Laser Versus Neodymium-Yttrium Aluminum: Garnet Laser Versus Intense Pulsed Light for the Treatment of Hirsutism Lasers are widely used for the treatment of hirsutism. But the choice of the right laser for the right skin type is very important. Before starting with laser therapy, it is important to assess the skin type, the fluence, the pulse duration and the type of laser to be used.To compare the efficacy and side effects of Diode laser, Neodymium-yttrium aluminum

2015 Journal of cutaneous and aesthetic surgery Controlled trial quality: uncertain

173. Blood Congestion Can Be Rescued by Hemodilution in a Random-Pattern Skin Flap. (Abstract)

subjected to a sham procedure. Subsequently, a random-pattern skin flap (1.5 × 6 cm) was elevated on the back of each rat. Physiologic assessments of flap vascularity/viability were performed using laser Doppler spectrophotometry before and after flap elevation.The normovolemic hemodilution group showed anemia (hemoglobin, 9.5 ± 0.8 g/dl) but less flow occlusion and greater flap survival (72.8 ± 8.6 percent) compared with control (57.4 ± 9.6 percent; p < 0.01) and blood transfusion (62.1 ± 6.5 percent (...) Blood Congestion Can Be Rescued by Hemodilution in a Random-Pattern Skin Flap. There is no standard method to ensure survival of random-pattern skin flaps. The authors developed a rat anemia model to observe survival of random-pattern skin flaps after blood transfusion and hemodilution.Anemia was induced by withdrawal of 35 percent blood volume followed by compensation with the same amount of blood (blood transfusion model) or plasma equivalent (normovolemic hemodilution). Control rats were

2017 Plastic and reconstructive surgery

174. Radio Frequency Microneedling for Suprapatellar Skin

procedures (e.g., laser or light treatments) for the treatment of wrinkles, skin resurfacing, or skin rejuvenation in the treatment area within 1 year of study participation. Contacts and Locations Go to Information from the National Library of Medicine To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor. Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03507036 Locations Layout table (...) of elastin. Additionally, as humans age, skin tends to appear more dry due to its poor hydration and turgor capacity. The use of minimally invasive aesthetic treatments in reducing signs of aging has been gaining in popularity over surgical treatments in recent years. Several energy types including, laser, radiofrequency, infrared, and ultrasound, have been developed for facial rejuvenation. These treatments induce controlled thermal damage into the dermis and cause collagen contraction

2017 Clinical Trials

175. Evaluation of the Efficacy and Safety of PiQo4 for Facial Skin Rejuvenation

. Condition or disease Intervention/treatment Phase Skin Rejuvenation Device: PiQo4 laser system Not Applicable Study Design Go to Layout table for study information Study Type : Interventional (Clinical Trial) Estimated Enrollment : 20 participants Intervention Model: Single Group Assignment Masking: None (Open Label) Primary Purpose: Treatment Official Title: Evaluation of the Efficacy and Safety of PiQo4 for Facial Skin Rejuvenation Actual Study Start Date : March 12, 2018 Estimated Primary Completion (...) Date : July 30, 2019 Estimated Study Completion Date : August 30, 2019 Arms and Interventions Go to Arm Intervention/treatment Experimental: Facial skin rejuvenation Facial skin rejuvenation using PiQo4 laser system Device: PiQo4 laser system The PiQo4 laser system Outcome Measures Go to Primary Outcome Measures : Fitzpatrick Elastosis Score (FES) scale [ Time Frame: Baseline, 1 month follow up ] Fine lines/wrinkles and elastosis improvement will be classified by the Fitzpatrick-Goldman Elastosis

2017 Clinical Trials

176. Study to Assess the Cosmetic Changes in the Facial Skin After Use of a Topical Retinoid Product in Participants With Moderate to Severe Photodamage

, rosacea, skin cancer, etc.) Individuals who require electrolysis, waxing, or use depilatories on the face during the study Chemical peel or microdermabrasion within 4 weeks of study start Retin-A®, Retin-A Micro®, Renova®, Avita®,Tazorac®, Avage® or Differin® or other similar prescription drugs within 3 months of study start Cosmetic injections (filler and/or toxins, i.e. Juvederm, Radiesse, Botox, etc.), non-ablative laser or fractional laser resurfacing Accutane® or other oral retinoid, Ablative (...) procedures (i.e. laser, chemical, cosmetic surgeries) within 12 months of study start Participants who have planned surgeries or procedures. Contacts and Locations Go to Information from the National Library of Medicine To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor. Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03302559 Locations Layout table for location information United

2017 Clinical Trials

177. Oily Skin: A review of Treatment Options Full Text available with Trip Pro

Oily Skin: A review of Treatment Options One of the most common dermatologic concerns is oily skin, and the demand for effective treatment options is ever apparent. This review article addresses numerous topical treatment options such as retinoids, olumacostat glasaretil, and various cosmeceutical agents. several systemic and procedural techniques that incorporate isotretinoin, spironolactone, oral contraceptives, botulinum toxin, photodynamic therapy, and lasers are reviewed as well. Each

2017 The Journal of clinical and aesthetic dermatology

178. Virus-Induced Cancers of the Skin and Mucosa: Are We Dealing with “Smoking Guns” or “Smoke and Mirrors” in the Operating Theatre? Full Text available with Trip Pro

Virus-Induced Cancers of the Skin and Mucosa: Are We Dealing with “Smoking Guns” or “Smoke and Mirrors” in the Operating Theatre? Human papillomavirus (HPV) alone is thought to cause ~610,000 cases of cancer per year, and is the dominant aetiological agent for ano-genital (esp. cervical) and head and neck cancers (esp. oropharyngeal). Merkel cell polyomavirus (MCV) is a more recently discovered virus which causes Merkel cell carcinoma, a rare but highly aggressive skin malignancy.We (...) explored the available published evidence to see if transmission of live HPV or MCV virus in smoke generated by laser or diathermy was feasible, and would pose an infection risk. Long-term infection with such carcinogenic viruses would then pose an increased risk for the development of virus-induced cancers in medical personnel.The morphological structures of both HPV and MCV are very similar, and the size, external capsids and genomic structures show striking similarity. Both viruses have a non

2017 Dermatology and therapy

179. Efficacy of Micro-excisional Skin Removal by Micro-coring Device in Treatment of Wrinkles and Laxity of Face and Neck

days before treatment or during the study period Contacts and Locations Go to Information from the National Library of Medicine To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor. Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03583918 Locations Layout table for location information United States, California Laser and Skin Surgery Center of Northern California Sacramento (...) , California, United States, 95816 United States, Florida Miami Dermatology and Laser Institute Miami, Florida, United States, 33173 United States, New York Laser and Skin Surgery Center of New York New York, New York, United States, 10016 United States, Tennessee The Practice of Brian S. Biesman, M.D Nashville, Tennessee, United States, 37203 United States, Texas Dr A Jay Burns Cosmetic Surgery Dallas, Texas, United States, 75231 Sponsors and Collaborators Cytrellis Biosystems, Inc. Investigators Layout

2017 Clinical Trials

180. VBeam Prima for Treatment of Photoaged Facial Skin

of ingesting medications known to induce photosensitivity, or history of seizure disorders due to light. Surgical, light-based therapy or RF procedures in the treatment area within 3 months of treatment or during the study. Any other surgery in the treated area within 3 months of treatment (or more if skin has not healed completely) or during the study. Tattoo or permanent make-up in the treated area. Systemica use of retinoids (i.e. Retin-A®, Accutane®) or antioxidants (i.e. Restylane®, Strivectin® (...) VBeam Prima for Treatment of Photoaged Facial Skin VBeam Prima for Treatment of Photoaged Facial Skin - 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. VBeam Prima for Treatment of Photoaged Facial Skin

2017 Clinical Trials

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