Clinical Trials Logo

Acne Vulgaris clinical trials

View clinical trials related to Acne Vulgaris.

Filter by:

NCT ID: NCT00818519 Completed - Acne Vulgaris Clinical Trials

GA YAZ ACNE in China Phase III

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

The purpose of this study is to evaluate the efficacy and safety of YAZ (drospirenone 3 mg / ethinylestradiol 20 µg) in comparison with placebo in female patients with moderate acne vulgaris over 6 treatment cycles.

NCT ID: NCT00814918 Withdrawn - Acne Vulgaris Clinical Trials

Topical 5-ALA-PDT With Blu-U Therapy Versus Topical 5-ALA With Pulse Dye Laser In Treating Recalcitrant Acne Vulgaris

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

The goal of this study is to compare how efficient two different types of PDTs are when used in combination with topical 5-ALA. The two types of PDT lights are Blu-U light and Candela V-beam Pulse Dye Laser.

NCT ID: NCT00807014 Completed - Acne Vulgaris Clinical Trials

Evaluation of Quality of Life, Efficacy, and Tolerance of Duac® Gel Compared to Differin® Gel in the Treatment of Acne

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

The objectives of this clinical trial are to compare the quality of life of the subjects, the efficacy and the tolerance of Duac® Gel (gel formulation with a combination of clindamycin phosphate [equivalent to 1% clindamycin] and 5% benzoyl peroxide), applied once daily, against Differin® Gel (gel with 0.1% adapalene), used once daily, in the treatment of mild to moderate acne vulgaris.

NCT ID: NCT00795327 Completed - Acne Vulgaris Clinical Trials

Injectable POLY-L-Lactic Acid for Treatment of Hill and Valley Acne Scarring

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

Primary: Evaluate the degree of correction attainable with Poly-L-Lactic Acid(Sculptra) for the correction of hill and valley acne scarring Secondary: Document types and incidence of device adverse events with Poly-L-Lactic Acid(Sculptra) therapy.

NCT ID: NCT00787943 Completed - Acne Vulgaris Clinical Trials

Study of Two Different 10.0% Benzoyl Peroxide Creams for Mild to Moderate Acne Vulgaris

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

This study is a split face, paired-comparison, pilot study of 10 subjects. 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 the clinic, as well as advertising and 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: NCT00776919 Completed - Acne Vulgaris Clinical Trials

Trial of Clindamycin / Benzoyl Peroxide Gel in Subjects With Acne

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

This is a Randomized, Double-Blind, Controlled Study to evaluate the Safety and Efficacy of a clindamycin / benzoyl peroxide gel in Subjects with Acne Vulgaris

NCT ID: NCT00767104 Completed - Acne Vulgaris Clinical Trials

Efficacy of Silk - Like Bedding Fabric Pillow Case in the Treatment of Acne Vulgaris

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

The purpose of this research study is to better understand how this study pillowcase works when people use it to treat acne. Most people, including people with acne, sleep six to eight hours each night in direct contact with bedding fabrics that provide no benefit to the healing process associated with acne. The fabric in this study pillowcase may be able to reduce bacteria on the skin. This study would evaluate how acne is affected by this silk-like pillowcase. This type of study has not been done before.

NCT ID: NCT00765375 Terminated - Acne Vulgaris Clinical Trials

Safety and Efficacy of the Use of Botox on Acne

Start date: September 2008
Phase: Phase 2
Study type: Interventional

• To determine the safety and efficacy of Botox Treatment in subjects with mild to moderate acne vulgaris defined by the Investigator's Global Assessment (IGA)

NCT ID: NCT00757523 Completed - Acne Vulgaris Clinical Trials

Evaluation of the Effectiveness, Safety, and Tolerability of Duac Akne Gel and Epiduo Gel in the Treatment of Facial Acne Vulgaris

Start date: September 10, 2008
Phase: Phase 4
Study type: Interventional

The purpose of this study is to compare the effectiveness of two marketed products in subjects with facial acne vulgaris

NCT ID: NCT00757315 Active, not recruiting - Clinical trials for Acne Keloidalis Nuchae

NdYag Laser for Acne Keloidalis Nuchae

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

Acne Keloidalis Nuchae (AKN) is a long standing hair follicle disease with bumps and scars on the skin of the back of the head and neck. The purpose of this new study is to determine how well a hair removal laser (NdYag Laser) works in treating AKN.