search

Active clinical trials for "Acne Vulgaris"

Results 91-100 of 597

Low Glycemic Index and Load Diet for the Treatment of Acne

Acne VulgarisDiet Modification

Clinical trial to determine the effect of adding a diet with low glycemic index and load to adults for the treatment of moderate acne. Adult patients with acne where recruited in two groups, A and B. Group A received a normal diet according to their metabolic status and group B received a diet with low glycemic index and load. Outcomes were measured at week 12.

Completed15 enrollment criteria

Bioequivalence Study of Two Treatments in the Treatment of Acne Vulgaris on the Face

Acne Vulgaris

To compare the safety and efficacy of Perrigo's product to an FDA approved product for the treatment of Acne Vulgaris

Completed18 enrollment criteria

A Pilot Study to Evaluate the Effect of a Probiotic Mixture in Acne

AcneAcne Vulgaris

A 12-week randomized, double-blind, placebo-controlled pilot study to evaluate the effect of a probiotic blend in the treatment and clinical and subjective evolution of acne vulgaris in adolescent and adult patients between 12 and 30 years.

Completed7 enrollment criteria

Pharmacokinetics and Safety of ALA in Acne Vulgaris

Acne Vulgaris

This study will evaluate the pharmacokinetics and safety of ALA in patients with moderate and severe acne vulgaris after single dose in different dosages.

Completed26 enrollment criteria

Tazarotene 0.045% Lotion for Treating PIE and PIH in Subjects With Acne

Acne VulgarisPost Inflammatory Hyperpigmentation3 more

The purpose of the study is to assess the safety and efficacy of Arazlo Lotion (Tazarotene 0.045% Lotion) for treatment of postinflammatory erythema and postinflammatory hyperpigmentation in subjects with acne.

Completed16 enrollment criteria

To Evaluate the Efficacy and Safety of Minocycline Hydrochloride Foam in the Treatment of Moderate-to-severe...

Acne Vulgaris

This is a randomized, multicenter, double-blind, vehicle-controlled, 2-arm study to evaluate the safety and efficacy in 12 weeks of FMX101 minocycline foam, 4%, compared to vehicle, in the treatment of subjects with moderate to severe facial acne vulgaris.

Completed9 enrollment criteria

Open-label Safety and Tolerability Study of LTS-PDT in Healthy Volunteers

Acne Vulgaris

The purpose of this study is assess the safety and tolerability of lemuteporfin topical solution (LTS) with exposure to red light (PDT), when applied to the backs of healthy volunteers.

Completed12 enrollment criteria

A Safety, Tolerability and Preliminary Efficacy Study of DRM01B Topical Gel

Acne Vulgaris

This is a Phase 1/2a study. The purpose of Phase 1 was to evaluate the safety and tolerability of DRM01B Topical Gel in 6 healthy volunteers. The purpose of Phase 2a was to assess the safety, tolerability and preliminary efficacy of DRM01B Topical Gel compared to vehicle in subjects with acne vulgaris on the face.

Completed48 enrollment criteria

Double-Blind, Placebo-Controlled Study to Evaluate 3 Doses of a Novel Tetracycline in the Treatment...

Acne Vulgaris

To evaluate the safety and effectiveness of 3 strengths of P005672-HCl compared to placebo for the treatment of moderate to severe facial acne vulgaris.

Completed21 enrollment criteria

Fractional Ablative Radiofrequency for the Treatment of Acne Scars and Wrinkles

WrinklesAcne Scars

To assess the safety and efficacy of the Pixel RF (fractional radio frequency) module in the treatment of acne scars and wrinkles.

Completed19 enrollment criteria
1...91011...60

Need Help? Contact our team!


We'll reach out to this number within 24 hrs