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Acne Vulgaris clinical trials

View clinical trials related to Acne Vulgaris.

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NCT ID: NCT04018885 Completed - Acne Vulgaris Clinical Trials

A Study on Safety and Preliminary Efficacy of ALA in Acne Vulgaris

Start date: July 11, 2019
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this study is to explore the safety, tolerability, and preliminary efficacy of ALA used with photodynamic therapy for the treatment of moderate to severe acne vulgaris.

NCT ID: NCT04015375 Completed - Acne Vulgaris Clinical Trials

Study Comparing Test to Aczone 7.5% and Both to a Placebo Control in the Treatment of Acne Vulgaris

Start date: July 11, 2019
Phase: Phase 3
Study type: Interventional

To evaluate the therapeutic effect of Dapsone and Placebo gel in the treatment of acne vulgaris.

NCT ID: NCT04002024 Completed - Acne Vulgaris Clinical Trials

Moisturizer Containing Licochalcone A, Decanediol, L-carnitine and Salicylic Acid in Reducing Relapsing of Acne

Start date: June 1, 2019
Phase: N/A
Study type: Interventional

Moisturizer containing the active ingredients of licochalcone A, decanediol, L-carnitine, and salicylic acid may be beneficial in alternative treatment of acne in maintenance phase. This study aims to evaluate the efficacy and safety of moisturizer containing the active ingredients of licochalcone A, decanediol, L-carnitine, and salicylic acid during the maintenance phase of acne in Thai patients.

NCT ID: NCT03938467 Completed - Clinical trials for Rate of Positive Culture Growth for C.Acnes From Specimens Obtained From the Shoulders of Patients Undergoing Primary Shoulder Arthroplasty

Irrisept C.Acnes Study

Start date: March 1, 2021
Phase: Phase 4
Study type: Interventional

A Prospective, Randomized, Controlled Trial Comparing An Irrisept Antiseptic Irrigation With 0.05% Chlorhexidine Gluconate versus Standard of Care Prophylaxis Chlorohexidine Wipes

NCT ID: NCT03933033 Completed - Acne Vulgaris Clinical Trials

Erbium-YAG Laser Versus Platelet Rich Plasma in the Treatment of Atrophic Acne Scars

Start date: June 1, 2017
Phase: N/A
Study type: Interventional

This study aim to assess the efficacy of Er-YAG laser 2940nm and PRP as a single line of treatment in comparison with combined treatment in atrophic post acne scars.

NCT ID: NCT03921476 Withdrawn - Acne Vulgaris Clinical Trials

Acne and Mood: Impact of Treatment on Depression, Anxiety, and Sexual Function

Start date: July 1, 2020
Phase:
Study type: Observational

This study seeks to examine if there is any relationship between spironolactone use prescribed for acne vulgaris and depression, anxiety, and/or sexual function.

NCT ID: NCT03915860 Completed - Acne Vulgaris Clinical Trials

Participant Reported Outcomes With Use of Trifarotene 50 μg/g Cream in the Treatment of Moderate Facial and Truncal Acne Vulgaris

Start date: March 27, 2019
Phase: Phase 3
Study type: Interventional

Participant Reported Outcomes with use of Trifarotene 50 μg/g Cream in participants with Moderate Facial and Truncal Acne Vulgaris

NCT ID: NCT03901417 Active, not recruiting - Acne Scars Clinical Trials

Comparison of 1550nm Fractional Laser Alone Versus in Combination With Microneedling for the Treatment of Acne Scars

Start date: June 1, 2019
Phase: N/A
Study type: Interventional

Acne scarring is an unfortunate consequence of inflammatory acne vulgaris that often leads to significant cosmetic and psychosocial impacts. Although there have been many advances in the treatment of acne scarring, it remains one of the greatest challenges in cosmetic and laser dermatology. There have been a multitude of studies establishing the efficacy of non-ablative fractional laser therapy for the treatment of atrophic acne scars, and it is widely regarded as one of the best available treatments. More recently, there has been a renewed interest in controlled, non-thermal dermal injury via microneedling devices in the treatment of atrophic acne scars. Where there is a gap in the literature, however, is in the evaluation of the combination of non-ablative fractional laser resurfacing with microneedling in the treatment of atrophic acne scars. The investigators' study will compare the safety and efficacy of using non-ablative fractional laser versus a combination of microneedling and non-ablative fractional laser for atrophic acne scars using a randomized, double-blind, split-face study. The investigators' aim is to further elucidate the pathogenesis of acne scarring and the best approaches for treatment. In doing so, the investigators will study a combination approach to this complex problem in order to better serve future patients.

NCT ID: NCT03900676 Active, not recruiting - Acne Vulgaris Clinical Trials

Efficacy and Safety Study of VB-1953 Topical Gel for Inflammatory Facial Acne Vulgaris

Start date: April 9, 2019
Phase: Phase 2
Study type: Interventional

A Phase 2, Multicenter, Randomized, Double-Blind, Vehicle Controlled, Dose-ranging Study in the Treatment of Acne Vulgaris,

NCT ID: NCT03883269 Recruiting - Acne Vulgaris Clinical Trials

Anti-inflammatory Effects of Topical Erythromycin and Clindamycin in Acne Patients

Start date: March 20, 2018
Phase: Phase 4
Study type: Interventional

The combined bacteriostatic and immunomodulatory effects of erythromycin and clindamycin will be explored. Treatment effects will be extensively characterized by conventional methods including lesion counts, global assessment scales and visual grading as well as state-of-the-art methodology, including multi-modal photo analysis, perfusion by laser speckle contrast imaging, analysis of local skin surface, biopsy biomarkers and skin microbiota. This extensive response profiling, combined with the mechanistic insights from concurrent in vitro and in vivo studies in healthy volunteer challenges, will increase the understanding of erythromycin's and clindamycin's effects in acne vulgaris.