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Active clinical trials for "Rosacea"

Results 131-140 of 196

Exploration of Safety and Efficacy of AzA 15% Foam Twice a Day in Rosacea

Papulopustular Rosacea

This exploratory study is being performed to determine whether a new form formulation of azelaic acid 15% is effective in the treatment of papulopustular rosecea.

Completed20 enrollment criteria

Systemic Bioavailability Study Of Col-118 Administered Topically as a 0.18 % Facial Gel And Brimonidine...

Erythematous Rosacea

Phase II systemic bioavailability crossover study to measure the exposure of Col-118 topical 0.18 % Facial Gel and Brimonidine Ophthalmic Solution 0.2%

Completed12 enrollment criteria

Isotretinoin in Papular-Pustular Rosacea

Papular-pustular Rosacea

A national, multicentre, prospective, randomised, double-blind, phase III study in 2 parallel groups of isotretinoin versus placebo in patients presenting papular-pustular rosacea resistant to standard therapy. A non-balanced group (2 isotretinoin /1 placebo) design was selected since, given the nature of the study disease, fewer patients will receive the placebo than active isotretinoin. Treatment duration for each patient : 4 months, with monthly evaluation Follow-up at 2 months and 4 months for patients responsive after 4 months of treatment.

Completed26 enrollment criteria

Pulsed Dye Laser (PDL) vs. Microsecond 1064-nm Nd:YAG Laser for Treatment of Diffuse Facial Redness...

Rosacea

The primary objective of this study is to compare the efficacy of PDL and the 1064-nm Nd:YAG laser in the treatment of facial redness.

Completed7 enrollment criteria

Efficacy of Topical Cyclosporin for Ocular Rosacea

Rosacea

The purpose of this study is to determine whether Restasis (topical cyclosporin) is effective in the treatment of ocular rosacea

Completed13 enrollment criteria

Open Label Phase 2 Feasibility Study of BPX-04 Topical Minocycline Gel in Rosacea

Moderate to Severe Papulopustular Rosacea

An open label feasibility study using BPX-04 topical minocycline gel in papulopustular rosacea.

Completed26 enrollment criteria

Safety and Efficacy Study of a Topical Minocycline Foam in Patients With Papulopustular Rosacea...

RosaceaPapulopustular Rosacea

The purpose of this study is to see if the study drug, FMX-103, is safe to give and if it helps people with moderate-to-severe papulopustular rosacea. The investigational product is FMX-103 minocycline foam. Two concentrations of the investigational product, 1.5% and 3%, will be studied along with vehicle. The foam will be applied once daily to the face for the 12-week treatment duration of the study. Approximately 210 patients will participate in this study.

Completed9 enrollment criteria

To Evaluate the Therapeutic Equivalence and Safety of Azelaic Acid 15% Topical Gel

Rosacea

A Multi-Center, Double-Blind, Randomized, Placebo Controlled, Parallel-Group Study

Completed3 enrollment criteria

Bioequivalence Study of Two Treatments in the Treatment of Inflammatory Lesions of Rosacea on the...

Rosacea

To compare the bioequivalence of Perrigo's azelaic acid foam product to Finacea Foam for the treatment of Inflammatory Lesions of Rosacea

Completed26 enrollment criteria

A Study of DER 45-EV Gel to Treat Rosacea

Rosacea

To identify lowest efficacious dose of DER 45 EV Gel, 1% and 5% verses vehicle in patients with rosacea.

Completed8 enrollment criteria
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