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Acne Vulgaris clinical trials

View clinical trials related to Acne Vulgaris.

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NCT ID: NCT00887484 Completed - Acne Vulgaris Clinical Trials

A Comparative Study of the Tolerability of Two Combination Therapies for the Treatment of Acne

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

The purpose of this study is to compare the tolerability of topical combination therapies in the treatment of facial acne.

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.

NCT ID: NCT00877409 Not yet recruiting - Acne Vulgaris Clinical Trials

Safety and Efficacy Study of Acnase Creme in the Treatment of Acne Vulgaris I and II

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

The objective of this study is to establish the safety in use of the topical drug Acnase Creme and its effectiveness in treatment of acne grade I (comedones) and II (comedones, papules, pustules).

NCT ID: NCT00869492 Active, not recruiting - Acne Vulgaris Clinical Trials

Comparison of Nadifloxacin Cream Alone and With Benzoyl Peroxide Solution in the Treatment of Acne

Start date: August 2008
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine whether using of nadifloxacine 1% cream and benzoyl peroxide 5% solution together is more effective than using nadifloxacine alone in the treatment of mild to moderate facial acne.

NCT ID: NCT00848744 Completed - Acne Vulgaris Clinical Trials

Comparison of Two Salicylic Acid Formulations

Start date: February 2008
Phase: N/A
Study type: Interventional

This study is a split face, paired-comparison, pilot study of at least 10 subjects to complete. Participants in this study will be patients seen at Children's Memorial Hospital, who are clinically diagnosed with mild to moderate acne vulgaris. Participants will be recruited from one of the clinics, as well as from previous Institutional Review Board (IRB) approved acne studies housed in the Department of Dermatology. All subjects accrued from previous studies have agreed to be contacted for further investigations. Subjects 13 to 35 years of age with mild to moderate acne vulgaris symmetrical in appearance on both sides of the face, and meeting inclusion criteria will be eligible to participate

NCT ID: NCT00841776 Completed - Acne Clinical Trials

Comparative Antimicrobial Efficacy of Two Topical Acne Therapies for the Treatment of Facial Acne

Start date: August 2007
Phase: Phase 4
Study type: Interventional

The purpose of the study is to determine the development of microbial resistance when using one of two topical acne therapies for the treatment of facial acne vulgaris.

NCT ID: NCT00838812 Completed - Acne Vulgaris Clinical Trials

Safety and Efficacy Study of Association Between Tretinoin and Clindamycin on the Treatment of Acne Mild and Moderate

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

The purpose of this study is to determine the safety and efficacy of association between tretinoin and clindamycin phosphate on the treatment of acne vulgaris mild and moderate.

NCT ID: NCT00835198 Completed - Acne Vulgaris Clinical Trials

Dapsone Gel 5% and Tretinoin Gel 0.025% Versus Tretinoin Gel 0.025% Monotherapy for Facial Acne Vulgaris

Start date: December 2008
Phase: Phase 4
Study type: Interventional

A 12-week evaluation of the safety and efficacy of dapsone gel 5% when used with tretinoin gel 0.025% compared with tretinoin gel 0.025% monotherapy in treating moderate to severe facial acne vulgaris

NCT ID: NCT00834210 Completed - Acne Vulgaris Clinical Trials

Dapsone Gel 5% and Tazarotene Cream 0.1% Versus Tazarotene Cream 0.1% Monotherapy for Facial Acne Vulgaris

Start date: December 2008
Phase: Phase 4
Study type: Interventional

A 12-week evaluation of the safety and efficacy of dapsone gel 5% when used with tazarotene cream 0.1% compared with tazarotene cream 0.1% monotherapy in treating moderate to severe facial acne vulgaris

NCT ID: NCT00829049 Terminated - Acne Vulgaris Clinical Trials

Safety and Efficacy of Tazarotene Cream 0.1% Compared With Adapalene Gel 0.3% in the Treatment of Moderate to Severe Facial Acne Vulgaris

Start date: October 2007
Phase: Phase 4
Study type: Interventional

Comparison of the safety and efficacy of Tazarotene Cream 0.1% compared with Adapalene Gel 0.3% in treating moderate to severe facial acne vulgaris