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Acne Vulgaris clinical trials

View clinical trials related to Acne Vulgaris.

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NCT ID: NCT00974870 Completed - Acne Scars Clinical Trials

A Pilot Study Testing the Efficacy of a Needling Device for the Treatment of Acne Scars

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

The primary objective of this study is to determine the efficacy of a needling device for treatment of acne scars.

NCT ID: NCT00964366 Completed - Acne Vulgaris Clinical Trials

Study to Determine and Compare the Tolerance and Irritation Potential of Topical Acne Medications

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

This is a randomized, half-face study. On 1 side of the face, the subject will apply 1 of the 2 test products, clindamycin and benzoyl peroxide or dapsone gel and the contra lateral side of the face will remain non-treated to serve as a control.

NCT ID: NCT00964223 Completed - Acne Vulgaris Clinical Trials

A Study to Evaluate Tolerability of Two Topical Drug Products in the Treatment of Facial Acne

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

Multi-center, single-blind, randomized, comparative, split-face study. The duration of the study is 8 weeks. Commencing at baseline, subjects will apply once daily both clindamycin and benzoyl peroxide gel and benzoyl peroxide/adapalene gel in a bilateral split-face fashion (allocation to left and right side randomly assigned) for an initial 2 weeks. After visit 3, subjects will commence application of clindamycin and benzoyl peroxide gel to the entire face for an additional 6 weeks.

NCT ID: NCT00952523 Completed - Acne Vulgaris Clinical Trials

Evaluation of Irritation That Potentially Could be Caused by Two Facial Gels Applied to Opposite Sides of the Face

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

A study to compare the skin irritation potential of two marketed gels for acne treatment, each applied to half of the face of healthy volunteers.

NCT ID: NCT00933543 Completed - Acne Vulgaris Clinical Trials

Efficacy and Safety Study With Visonac Photodynamic Therapy (PDT)

Start date: August 2009
Phase: Phase 2
Study type: Interventional

The purpose of this trial is to study the efficacy and safety of Visonac PDT in patients from 9 to 35 years old with Aktilite® CL512. Patients was randomized to Visonac or vehicle cream without occlusion and red light(dose: 37J/cm2)

NCT ID: NCT00926367 Completed - Acne Vulgaris Clinical Trials

Two-week Study to Compare the Tolerance and Irritation Potential of Two Combination Topical Gel Acne Medications

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

This is a single-blind (blinded expert grader), randomized, half-face study being conducted at one clinical site. On 1 side of the face, the subject will apply 1 of the 2 test products, antibiotic and benzoyl peroxide or benzoyl peroxide and adapalene gel and the contra lateral side of the face will remain non-treated to serve as a control. Approximately 25-30 male and female healthy subjects will be randomly assigned to each product

NCT ID: NCT00919191 Completed - Acne Vulgaris Clinical Trials

Evaluation of Irritation by Two Facial Gels Applied to Opposite Sides of the Face

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

A study to compare the skin irritation potential of two marketed gels for acne treatment, each applied to half of the face of healthy volunteers.

NCT ID: NCT00907335 Completed - Acne Vulgaris Clinical Trials

A Study of Acne Treatment in Children Ages 9 to 11

Start date: February 2009
Phase: Phase 2
Study type: Interventional

A study to determine if using Retin-A Micro 0.04% as facial acne treatment in patients ages 9 to 11 is safe and efficacious.

NCT ID: NCT00907257 Completed - Acne Vulgaris Clinical Trials

A Study of Different Use Regimens Using Two Acne Treatments

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

A study to determine if using 2 acne products in the morning is as safe and efficacious as using one product in the morning and one product in the evening.

NCT ID: NCT00907101 Completed - Clinical trials for P Acnes Colonization

Evaluate Effectiveness of Epiduo® Gel in Reducing Antibiotic Sensitive & Resistant Strains of Propionibacterium (P)Acnes

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

The purpose of this study is to evaluate the effectiveness of Epiduo® Gel in reducing antibiotic sensitive and resistant strains of P acnes in vivo.