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Acne clinical trials

View clinical trials related to Acne.

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NCT ID: NCT01162837 Completed - Acne Clinical Trials

Safety & Effectiveness of the BEAM Device in Mild-to-moderate Acne

Start date: June 2010
Phase: N/A
Study type: Interventional

This study will determine if the use of the BEAM device reduces the signs and symptoms of mild-to-moderate acne.

NCT ID: NCT01138735 Completed - Acne Clinical Trials

Epiduo Pediatric Acne Study

Start date: June 2010
Phase: Phase 4
Study type: Interventional

The purpose of this study is to evaluate the safety and efficacy of Epiduo® (adapalene and benzoyl peroxide) Gel 0.1%/2.5% administered once daily for up to 12 weeks in subjects 9 to 11 years of age with acne vulgaris.

NCT ID: NCT01135069 Completed - Acne Clinical Trials

Bioequivalence Study of Generic Tretinoin 0.1% Microsphere Gel, 0.1% Retin-A Micro® and Placebo

Start date: October 2009
Phase: Phase 3
Study type: Interventional

The objective will be to assess clinical bioequivalence of 0.1% Retin-A Micro® Gel and Spear Pharmaceutical's generic 0.1% Tretinoin Microsphere Gel with a placebo arm.

NCT ID: NCT01106807 Completed - Acne Clinical Trials

Exploratory Study to Evaluate the Efficacy and Safety of CD07223 Gel in Subjects With Acne

Start date: April 2010
Phase: Phase 2
Study type: Interventional

The purpose of the study is to evaluate the efficacy of CD07223 1.5% Gel and 0.5% gel in reducing inflammatory, non-inflammatory, and total acne lesion counts after 6 weeks of twice daily applications. The study will also evaluate the safety of the study products using tolerance and adverse event data.

NCT ID: NCT01082523 Completed - Acne Clinical Trials

"A Randomized, Controlled, Evaluator-blinded Pilot Study to Evaluate the Effect of Automated Text Message Reminders on Patient Compliance With Topical Medications and Its Efficacy on Skin Disease Control in Adolescents and Adults With Mild to Moderate Acne"

Start date: February 2010
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether an automated electronic reminder system using text messages sent to patient's cell phones will help patients with acne be more compliant with their topical medications and lead to an improvement of their acne. Hypothesis: Automatically delivered electronic reminders in the form of text messages will increase acne patient adherence to topical medications and consequently result in better treatment outcome and higher patient satisfaction

NCT ID: NCT00998257 Completed - Contraception Clinical Trials

Regulatory Post Marketing Surveillance Study on YAZ

Start date: July 2009
Phase: N/A
Study type: Observational

The objective of this Post Marketing Surveillance (PMS) is to gain information about safety and efficacy in real practice.

NCT ID: NCT00939133 Completed - Acne Clinical Trials

Proof of Concept Study to Investigate the Recurrence of Acne Post Isotretinoin

Start date: July 2009
Phase: Phase 4
Study type: Interventional

The use of topical retinoids is a mainstay and basis of early acne treatment to prevent the progression to inflammatory lesions. Post oral isotretinoin, it is not uncommon for non-inflammatory papules and comedones to recur. However, there has been no formal study to look at the prevention of recurrence of these acne lesions post isotretinoin in a long term basis. This may enhance the therapeutic options for post isotretinoin patients in order to prevent recurrence of their disease. Hypothesis Tretinoin microsphere 0.04% will prevent recurrence of acne lesions.

NCT ID: NCT00913185 Completed - Acne Clinical Trials

Comparison Study of Topical Acne Regimens

Start date: December 2006
Phase: Phase 4
Study type: Interventional

The purpose of this study is to compare the effectiveness of two over the counter acne products in subjects with moderate severity acne vulgaris. The two products being compared in this study are Acne Free "Severe Acne Line" manufactured by University Medical Products, and Proactiv® manufactured by Guthy-Renker.

NCT ID: NCT00900939 Completed - Acne Clinical Trials

Plant-based Dietary Intervention for Treatment of Acne

Start date: July 2009
Phase: N/A
Study type: Interventional

The purpose of this study is to determine if a low-fat, vegan diet affects the number of acne lesions, acne severity, and acne extent.

NCT ID: NCT00883233 Completed - Acne Clinical Trials

Comparison of Four Different Regimens of Adapalene 0.1% / Benzoyl Peroxide 2.5% Gel in Acne Vulgaris

FREE
Start date: April 2009
Phase: Phase 3
Study type: Interventional

The purpose of this study is to compare the tolerability of 3 treatment regimens containing Adapalene 0.1% / Benzoyl Peroxide 2.5% Gel with that of Adapalene 0.1% /Benzoyl Peroxide 2.5% Gel standard daily overnight application for 12 weeks in the treatment of acne vulgaris. The efficacy of the four treatment regimens will also be evaluated.