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Laser Skin Procedure

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141. Pilot Study of Multi-wavelength Laser for Tattoo Removal

Pilot Study of Multi-wavelength Laser for Tattoo Removal Pilot Study of Multi-wavelength Laser for Tattoo Removal - 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. Pilot Study of Multi-wavelength Laser (...) provided by (Responsible Party): Cutera Inc. Study Details Study Description Go to Brief Summary: To evaluate the safety and efficacy of an investigational version of the Cutera enLighten laser that offers muliple wavelengths for tattoo removal. Condition or disease Intervention/treatment Phase Tattoo Removal Device: Cutera enLighten laser Not Applicable Detailed Description: Currently, the enLighten laser offers two wavelengths: 532nm KTP and 1064nm Nd:YAG. The version of the laser under investigation

2017 Clinical Trials

142. Effect of LASER Photobiomodulation Therapy on Chronic Pain and Opioid Weaning

Study Completion Date : March 2019 Resource links provided by the National Library of Medicine related topics: Arms and Interventions Go to Arm Intervention/treatment ABAB Treatment, either LASER (arm A) or LOW LEVEL LASER (arm B) will be provided 3 (not less than 2) days a week for three weeks at which time crossover into the alternate arm occurs (BABA to ABAB or ABAB to BABA). ABAB initial period is active treatment - LASER. Active Treatment: LASER light is delivered to the skin and deeper tissues (...) affected by pain using either a wand or glass roller ball. Ten to 25 Watts of LASER energy is delivered to the painful regions for 8 to 16 minutes depending on the size of the area treated and other factors such as skin pigmentation. Device: LightForce EXPi LASER photobiomodulation therapy of 15-25 watts of coherent infrared light to affected area for 10 minutes using wand-type probe. Other Names: LASER photobiomodulation therapy LASER therapy BABA Treatment, either LASER (arm A) or LOW LEVEL LASER

2017 Clinical Trials

143. Laser Fluorescence in Cancer Surgical Treatment

, the present technology having a relevant role in intraoperative decision making. In the same year, Newman et al. The first application of the system in breast reconstruction surgery. In an initial series of 10 consecutive cases of reconstruction with microsurgical flaps, in 4 cases the system allowed the intraoperative identification of areas of low perfusion, thus changing the surgical procedure. According to the authors, there was a 95% correlation between indocyanine laser assisted and subsequent (...) development of mastectomy skin necrosis, with sensitivity of 100% and specificity of 91%. Similarly, Murray et al. Evaluated the intraoperative perfusion, however, of the areola-papillary complex in patients submitted to subcutaneous mastectomies with satisfactory results in terms of predictability of cutaneous circulation. Other authors in larger clinical series and evaluating other procedures have observed valid results in terms of prevention of complications. Vascular perfusion of anastomoses

2017 Clinical Trials

144. Cranial Laser Reflex Technique for Hamstring Function

Translational and Clinical Sciences Institute National Institutes of Health (NIH) Information provided by (Responsible Party): University of North Carolina, Chapel Hill Study Details Study Description Go to Brief Summary: Purpose: To conduct a pilot study of the effect of Cranial Laser Reflex Technique (CLRT) compared with sham laser on hamstring muscle flexibility, strength, and pain pressure threshold. Participants: Active, young adults ages 18 to 35. Procedures: A two-visit, assessor and participant (...) reflex points that modulate muscle tone. Other Name: Cranial Laser Reflex Technique Sham Comparator: Sham, Then CLRT The Sham procedure was identical to CLRT except the laser device was placed in placebo mode: all device indicator lights and sounds will be functional but no laser light will be emitted from probe aperture. Device: CLRT CLRT is a novel method of laser stimulation on specific cranial reflex points that modulate muscle tone. Other Name: Cranial Laser Reflex Technique Outcome Measures Go

2017 Clinical Trials

145. A Study to See if Low Level Laser Light Can Help to Treat Toenail Fungus

leaving the skin and surrounding healthy tissue unharmed. Low level laser therapy operates under the principle of photochemistry with a photoacceptor molecule absorbing the emitted photons and inducing a biological cascade. Like our eukaryotic cell, fungi contain the highly complex organelle the mitochondria, which is responsible for the manufacturing of the energy molecule adenosine triphosphate (ATP). Within the inner mitochondrial membrane is cytochrome c oxidase, an identified photoacceptor (...) A Study to See if Low Level Laser Light Can Help to Treat Toenail Fungus A Study to See if Low Level Laser Light Can Help to Treat Toenail Fungus - 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 Study

2017 Clinical Trials

146. Study of Laser Interstitial Thermal Therapy (LITT) in Recurrent Glioblastoma

thinks it may be in your best interest to also have a surgical procedure called laser interstitial thermal therapy (LITT). LITT is a minimally invasive (using small incisions) surgery method that uses lasers to destroy tumor cells. For the procedure, the study doctor uses the NeuroBlate system to perform LITT in combination with MRIs and software models to focus the lasers on affected brain cells. The goal of this clinical research study is to learn if the NeuroBlate system in combination (...) . The study doctor can describe how the study drug and procedure are designed to work. Up to 34 participants will be enrolled in this study. All will take part at MD Anderson. Condition or disease Intervention/treatment Phase Malignant Neoplasms of Eye Brain and Other Parts of Central Nervous System Glioblastoma Anaplastic Astrocytoma Procedure: Laser Interstitial Thermal Therapy Drug: Lomustine Behavioral: Quality of Life Questionnaires Device: The NeuroBlate System Phase 2 Study Design Go to Layout

2017 Clinical Trials

147. Efficacy and Safety of Picosecond, Neodymium-doped Yttrium Aluminum Garnet Laser Therapy Using 1,064 nm and 595 nm

influence the results of the clinical study. Agreed not to undergo any other procedure on their face during their participation in the clinical trial Voluntarily agreed to sign the written consent form and willing to follow the instructions of the study protocol Exclusion Criteria: Participated in another medical device or medication clinical trial in the last 3 months, or planning to participate in another trial during this trial Received a cosmetic treatment such as laser, light therapy, or surgery (...) Efficacy and Safety of Picosecond, Neodymium-doped Yttrium Aluminum Garnet Laser Therapy Using 1,064 nm and 595 nm Efficacy and Safety of Picosecond, Neodymium-doped Yttrium Aluminum Garnet Laser Therapy Using 1,064 nm and 595 nm - 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

2017 Clinical Trials

148. Platelet Rich Plasma, Complex Decongestive Physiotherapy and Low Level Laser in Treatment of Lower Extremity Lymphoedema

. This will be activated by the addition of platelet agonists such as thrombin, calcium gluconate or calcium chloride. Injections should be administered subcutaneously for 2-3 weeks, 3-4 times for inguinal, popliteal region and ankle for a total of 12 weeks. Also, all patients in this groups have received Complex Decongestive Physiotherapy (Manual lymph drainage (MLD), skin care, compression therapy and active therapeutic exercise). Experimental: Complex Decongestive Physiotherapy Procedure: Low Level Laser Low (...) for the inguinal region and the legs free in the abdomen.Also, all patients in this groups have received Complex Decongestive Physiotherapy (Manual lymph drainage (MLD), skin care, compression therapy and active therapeutic exercise). Experimental: Low Level Laser Procedure: Complex Decongestive Physiotherapy Complex Decongestive Physiotherapy (CDP) consists of four basic components and two phases. Four basic components; Manual lymph drainage (MLD), skin care, compression therapy and therapeutic exercise

2017 Clinical Trials

149. Low Level Laser Therapy Effects in Peripheral Nerves Patient With Leprosy.

and Interventions Go to Arm Intervention/treatment Sham Comparator: Control Leprosy patients with focal demyelinating neuropathy in compression sites of the ulnar and common peroneal nerves who will receive application "sham LLLT". The laser will be turned off, but the procedure will be the same as with the Low Level Laser Therapy (LLLT) group Device: Sham LLLT That group receive application "sham LLLT". The laser will be turned off, but the procedure will be the same as with the LLLT group Experimental: Low (...) Level Laser Therapy Leprosy patients with focal demyelinating neuropathy in compression sites of the ulnar and common peroneal nerves who will receive intervention with low-intensity laser therapy (LLLT). Device: LLLT The LLLT will be applied using a diode laser device (Recover Laser MMOptics, São Carlos/SP- Brazil) with parameters: 808nm, continuous output, 100mW, 8J. Laser probe will be applied directly and perpendicularly in skin contact (5 points), the time of irradiation will be 80 seconds per

2017 Clinical Trials

150. Use of Topical Liquid Diclofenac Following Laser Microporation of Cutaneous Neurofibromas in Patients With NF1

Use of Topical Liquid Diclofenac Following Laser Microporation of Cutaneous Neurofibromas in Patients With NF1 Use of Topical Liquid Diclofenac Following Laser Microporation of Cutaneous Neurofibromas in Patients With NF1 - 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. Use of Topical Liquid Diclofenac Following Laser Microporation of Cutaneous Neurofibromas in Patients With NF1 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: NCT03090971 Recruitment Status : Completed First Posted : March 27, 2017 Last

2017 Clinical Trials

151. Comparison of the Effect of Vaseline and Bepanthen® "Wund- Und Heilsalbe" on the Wound Healing Following Laser Therapy

of a laser treatment are strongly determined by an appropriate treatment with special skin care products of the laser-treated skin. Cooling measures prevent the swelling of the treated skin area, if applied directly after the procedure. A soothing and wound-healing-promoting care applied subsequently for seven days, can support and also speed up the healing process. The Lumenis® Company is the manufacturer of CO2 laser systems and recommends the application of the Okklusiv ointment Vaseline® (...) First Posted : March 30, 2017 Last Update Posted : May 30, 2018 Sponsor: RWTH Aachen University Information provided by (Responsible Party): RWTH Aachen University Study Details Study Description Go to Brief Summary: In the field of dermatology the healing process and therefore the success of a laser treatment are strongly determined by an appropriate postoperative treatment of the laser-treated skin. The manufacturer of CO2 laser systems recommends the application of Vaseline postoperatively

2017 Clinical Trials

152. Fractional Carbon Dioxide Laser,Topical Corticosteroid and Narrow Band Ultraviolet B in Treatment of Stable Vitiligo

in order to perform the procedures. Fractional carbon dioxide lasers, originally developed for tissue rejuvenation and scar remodeling. Recently, it has been used in the treatment of vitiligo. The newly developed fractional carbon dioxide laser does not ablate the entire epidermis, leaving intact skin between coagulated necrotic columns. It decreases risk of potential side effects and minimizes duration of sick leave. Several mechanisms may contribute to explain the improvement of Vitiligo after (...) . it is the most common depigmentation disorder, affecting approximately 0.5 to 2.0 percent of the population and has no predilection for gender or race . Condition or disease Intervention/treatment Phase Vitiligo Procedure: fractional carbon dioxide(CO2) laser Drug: Topical corticosteroid Radiation: Ultraviolet B narrow band Not Applicable Detailed Description: Vitiligo is primarily a clinical diagnosis without the need for diagnostic tools. It classified into three types: segmental vitiligo , nonsegmental

2017 Clinical Trials

153. Hybrid Fractional Laser for Symptoms of Genitourinary Syndrome of Menopause

) and 1470 nm diode lasers are cleared by the Food and Drug Administration (FDA) for ablation, vaporization, coagulation of soft tissue and for skin resurfacing. Fractional delivery of laser is a well-established method that stimulates tissue remodeling in the dermis while leaving the surrounding tissue intact in order to decrease healing time. The layers of skin and vaginal mucosal tissue exhibit similarities that suggest the clinical results seen with skin resurfacing may be translated to the vaginal (...) Hybrid Fractional Laser for Symptoms of Genitourinary Syndrome of Menopause Hybrid Fractional Laser for Symptoms of Genitourinary Syndrome of Menopause - 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. Hybrid

2017 Clinical Trials

154. Efficacy of 595 nm Pulsed-dye Laser in Treatment of Discoid Lupus Erythematosus

point Dose not undergo any procedure or laser treatment within 4 weeks before entered the study Dose not received any localised therapy of DLE eg. topical corticosteriod/immunomodulator within 4 weeks before entered the study Dose not receive the topical chemical peeling within 4 weeks before entered the study Has already received at least 1 systemic standard treatment for DLE and continue until the rest of the study Can follow the study's protocol Exclusion Criteria: Pregnancy or lactation History (...) Efficacy of 595 nm Pulsed-dye Laser in Treatment of Discoid Lupus Erythematosus Efficacy of 595 nm Pulsed-dye Laser in Treatment of Discoid Lupus Erythematosus - 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

2017 Clinical Trials

155. Efficacy of Laser Debridement on Pain and Bacterial Load in Chronic Wounds

distress in patients with chronic wounds, in efforts to expedite the wound healing process. Condition or disease Intervention/treatment Phase Wound Open Chronic Venous Hypertension (Idiopathic) With Ulcer Diabetic Foot Ulcer Device: Erbium:Yttrium-Aluminum-Garnet (Er:YAG) Laser Debridement Procedure: Scalpel/Curette Debridement Not Applicable Detailed Description: Chronic wounds are a debilitating affliction, affecting a substantial portion of the population worldwide and incurring staggering (...) , lasers have been successfully utilized in many fields of medicine. Lasers for wound debridement began in the 1970s, with the successful report of a continuous-beam carbon dioxide (CO2) laser used for skin graft preparation of infected decubitus ulcers (11). Laser debridement is based on the controlled vaporization of the superficial layers of the wound bed. This results in the removal of the tissue containing unwanted microbial and necrotic particles. The laser type and the number of passes performed

2017 Clinical Trials

156. Hybrid Fractional Laser Treatment for Symptoms of Urinary Incontinence

are cleared by the Food and Drug Administration (FDA) for ablation, vaporization, coagulation of soft tissue and for skin resurfacing. Fractional delivery of laser is a well-established method that stimulates tissue remodeling in the dermis while leaving the surrounding tissue intact in order to decrease healing time. The layers of skin and vaginal mucosal tissue exhibit similarities that suggest the clinical results seen with skin resurfacing may be translated to the vaginal tissue. Improved vaginal (...) Hybrid Fractional Laser Treatment for Symptoms of Urinary Incontinence Hybrid Fractional Laser Treatment for Symptoms of Urinary Incontinence - 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. Hybrid

2017 Clinical Trials

157. Ascorbic Acid Versus Diode Laser in the Treatment of Gingival Hyperpigmentation

Gingival Hyperpigmentaion Drug: Ascorbic Acid 500 MG Device: diode laser Phase 4 Detailed Description: Cosmetic dentistry is usually centered on aesthetic restorative procedures but it may also involve the appearance of the gingiva, especially when it is located in the anterior labial region. Oral pigmentation may be physiological or pathological in nature. Better esthetics results of depigmentation were achieved with diode laser than conventional scalpel and with rotary abrasion, also diode laser (...) 17, 2017 Last Update Posted: August 22, 2017 Last Verified: August 2017 Layout table for additional information Studies a U.S. FDA-regulated Drug Product: No Studies a U.S. FDA-regulated Device Product: No Keywords provided by Dalia Yosri, Ain Shams University: ascorbic acid diode laser gingival hyperpigmentation Additional relevant MeSH terms: Layout table for MeSH terms Hyperpigmentation Pigmentation Disorders Skin Diseases Ascorbic Acid Antioxidants Molecular Mechanisms of Pharmacological

2017 Clinical Trials

158. Laser Acupuncture for Dry Eye

Study Description Go to Brief Summary: Subjects with dry eye are enrolled at two ophthalmic centers and randomly assigned to a laser acupuncture group and control group under conventional treatment with artificial tears. The effects of laser acupuncture therapy for patients with dry eye are investigated. Condition or disease Intervention/treatment Phase Dry Eye Procedure: Laser acupuncture Procedure: Sham laser acupuncture Not Applicable Detailed Description: Objective: Dry eye is a common (...) : July 31, 2019 Resource links provided by the National Library of Medicine related topics: Arms and Interventions Go to Arm Intervention/treatment Experimental: Laser acupuncture The subjects are treated at acupoints including BL2, TE23, ST2, LI4, ST36, and GB37 using laser acupuncture during 3 sessions per week for 12 weeks. Procedure: Laser acupuncture Subjects were treated 3 times per week for 12 weeks with the LaserPen (GaAlAs laser diode, 810 nm, 150 mW, pulsed waves), which delivered 0.375 J

2017 Clinical Trials

159. Evaluation of Safety of Low Level Laser Device Treatment in Chronic Wounds

will be used to treat the experimental group. Along with the active LLLT, generally accepted standard wound care procedures will be used during the clinical trial by a qualified study nurse or doctor. These procedures will include wound cleaning and drying before irradiation with the laser device (sham or active). Each ulcer will be also assessed and debrided if needed. After irradiation, each ulcer will be dressed with saline gauze dressing and offloaded. Sham Comparator: Control group The control group (...) Volunteers: No Criteria Inclusion Criteria: Provide signed and dated Informed Consent Form Willing to comply with all study procedures and be available for the duration of the study Male or female, aged 18 to 90 Having a DFU of at least 3 months duration that had not improved after prior standard wound treatments HbA1c of <11.0 Size of wounds: 1-10 cm2 Having DFU of grades 2 or 3 according to Wagner's classification Exclusion Criteria: Immeasurable wounds or wounds that are unsuited to this laser

2017 Clinical Trials

160. Femtosecond Laser-assisted Corneal Debridement for Herpes Simplex Keratitis

, 2018 See Sponsor: Chunxiao Wang Information provided by (Responsible Party): Chunxiao Wang, Sun Yat-sen University Study Details Study Description Go to Brief Summary: The purpose of the study is to learn if adding femtosecond laser-assisted corneal debridement to a standard therapy of oral ganciclovir can help shorten the healing time of herpes simplex epithelial keratitis (HSK). Condition or disease Intervention/treatment Phase Herpes Simplex Keratitis Procedure: FLDEB Drug: Ganciclovir (GCV (...) : December 30, 2018 Estimated Study Completion Date : December 30, 2019 Resource links provided by the National Library of Medicine related topics: related topics: available for: Arms and Interventions Go to Arm Intervention/treatment Experimental: FLDEB combined with GCV orally Femtosecond laser-assisted cornea debridement (FLDEB) combined with ganciclovir (GCV) orally. Procedure: FLDEB The eye will be anesthetized, and femtosecond laser technology will be used to remove epithelial tissue (diameter: 8mm

2017 Clinical Trials

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