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Acne Vulgaris clinical trials

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NCT ID: NCT04167982 Recruiting - Acne Clinical Trials

Efficacy and Safety of Painless 5-aminolevulinic Acid Photodynamic Therapy for Moderate and Severe Acne Vulgaris

Start date: March 28, 2020
Phase: N/A
Study type: Interventional

This study is being done to compare a new, continuous illumination and short Incubation time regimen of 5-aminolevulinic acid photodynamic therapy (painless ALA- PDT) to low-dose and conventional dose of oral isotretinoin for treatment of moderate or severe acne vulgaris. The hypothesis is that the painless ALA- PDT will be equally or more efficacious as oral isotretinoin, and taking effect more quickly with less adverse effect.

NCT ID: NCT04060160 Recruiting - Acne Vulgaris Clinical Trials

Acne Detection Software (AcneDect)

AcneDect
Start date: October 29, 2020
Phase:
Study type: Observational

This study is to create a self-learning software that can detect acne lesions. Patients take a picture of their face every single day for 3 months with a secure mobile phone and fill out a pre-designed questionnaire. After 3 months, the mobile will be collected back and the pictures will be evaluated by 3 dermatologists. The software is able to learn from the dermatologists' evaluation and -using machine learning- a mechanism that should be able to automatically detect acne to some extent will be established.

NCT ID: NCT04028401 Recruiting - Clinical trials for Cutibacterium Acnes Infection

Optimization of Skin Preparation to Reduce Cutibacterium Acnes Colonization in Superficial and Deep Samples During Prosthetic Shoulder Surgery in Male Patients

OPRICA
Start date: June 19, 2020
Phase: Phase 3
Study type: Interventional

Infections on joint replacements remain one of the most serious complications of orthopaedic surgery. Despite improvements in skin preparation and antibiotic prophylaxis procedures, the risk of infection of joint prosthesis is still high, particularly for shoulder prostheses, especially in men. One of the bacteria most often involved in post-operative infections for shoulder prosthesis is Cutibacterium acnes (CA). This bacterium is one of the predominant bacteria in pilosebaceous units. Eradication of this micro-organism remains difficult despite the techniques used in the preoperative phase. The objective of this protocol is to evaluate the efficacy of applying a 5% benzoyl peroxide topical during the 5 days preceding the procedure in the surgical skin incision area, which is based on local acne treatment, on the reduction of the CA bacterial load in the dermis of the approach to shoulder arthroplasty in men.

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.

NCT ID: NCT03469076 Recruiting - Acne Vulgaris Clinical Trials

Studying the Skin Microbiome and the Potential of a Topical Probiotic Cream for Patients With Acne

Start date: April 25, 2016
Phase: N/A
Study type: Interventional

In this study the topical use of cream with live probiotic bacteria was evaluated for its efficacy in reducing acne symptoms and its effect on the skin microbiota on patients with acne. Patients with mild to moderate acne used the probiotic cream for 8 weeks and clinical evaluation and sampling was done at start, 4, 8 and 10 weeks. Next-Generation Sequencing was used to analyze the skin microbiota of the patients.

NCT ID: NCT03465150 Recruiting - Acne Clinical Trials

Creation of a Monocentric Cohort of Patients Treated for Acne at the Nantes University Hospital

COPACNE
Start date: September 23, 2018
Phase:
Study type: Observational [Patient Registry]

With 24 million results associated with Google's searchon keywords "severe acne", Pr Dreno's team understand better thatthis disease, which affects many French people, is a real concern of Public Health and not a "forced evil" of the adolescent period, which will eventually resolve itself. Acne does not affect the vital prognosis, but its psychosocial impact is major and should not be underestimated. Paradoxically, despite the high prevalence of acne, few quality epidemiological studies have been published. Physicians are often helpless when faced with patients' questions. They often need a lot of explanations, especially on the factors aggravating this dermatosis, which greatly affects their quality of life. This cohort, the first of its kind in France, will determine the predictive factors of therapeutic response, endogenous and environmental factors impacting on the severity of acne assess the quality of life and psychological impact of acne patients, determine the patient's course of care and the associated costs. Pr Dreno's team will also build up a bio collection (bacteriological samples).

NCT ID: NCT03264287 Recruiting - Acne Vulgaris Clinical Trials

Efficacy of Acupuncture Combined With Moving Cupping and Ear Point Tapping for Moderate and Severe Acne Vulgaris

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

This trial is designed to evaluate the efficacy of different frequencies in treating the moderate and severe acne vulgaris using acupuncture combined with moving cupping and ear point tapping.

NCT ID: NCT01969175 Recruiting - Acne Vulgaris Clinical Trials

Effect of a Low-glycemic-load and Milk-free Diet on Acne Severity

Start date: October 2013
Phase: N/A
Study type: Interventional

The objective of this study is to assess the effect of a low-glycemic-load and milk-free diet on acne severity. IGF-1 and a phosphorylated product of the mTORC pathway (p70S6K) will be assessed in both groups to explore the mTORC signaling pathway, which is thought to be related to clinical improvement in previous studies.

NCT ID: NCT01422785 Recruiting - Acne Vulgaris Clinical Trials

A Study Comparing Combination Clindamycin Phosphate/Tretinoin Gel Alone Versus With Benzoyl Peroxide Foaming Cloths for Facial Acne

Start date: July 2011
Phase: Phase 4
Study type: Interventional

There are many different factors that cause acne. So combination treatment using different medications that can address these different factors is commonly used to treat acne. Fixed-dose combination clindamycin phosphate 1.2% and tretinoin 0.025% gel and benzoyl peroxide 6% foaming cloths are both used to treat acne. This study will evaluate the use of the medications when used together.

NCT ID: NCT01301586 Recruiting - ACNE VULGARIS Clinical Trials

A Novel Combination Oral Agent to Treat Acne Vulgaris

Start date: November 2010
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this study is to evaluate a novel, combination product for the treatment of acne vulgaris in females