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Rosacea clinical trials

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NCT ID: NCT02393937 Completed - Clinical trials for Papulopustular Rosacea

A Therapeutic Equivalence Study of Two Metronidazole Gel 1% Topical Treatments of Rosacea

Start date: February 2015
Phase: Phase 3
Study type: Interventional

The purpose of this study is to compare the efficacy of two Metronidazole Gels 1%, in the treatment of Rosacea.

NCT ID: NCT02385240 Completed - Rosacea Clinical Trials

Comparative Safety and Efficacy of Two Rosacea Products in the Treatment of Facial Erythema of Rosacea

Start date: March 2015
Phase: Phase 3
Study type: Interventional

To compare safety and efficacy of Perrigo's rosacea drug product compared to an FDA approved rosacea drug product in the treatment of facial erythema of rosacea.

NCT ID: NCT02300129 Completed - Rosacea Clinical Trials

Effect of CD07805/47 Gel in Rosacea Flushing

Start date: April 2014
Phase: Phase 2
Study type: Interventional

Phase IIa study to assess the efficacy and safety of CD07805/47 0.5% gel in the treatment of the flush of rosacea.

NCT ID: NCT02292836 Completed - Rosacea Clinical Trials

Rosacea Prevalence in General Population - Pilot Study

Start date: August 2012
Phase: N/A
Study type: Observational

The purpose of this study is to test and refine, a subject questionnaire aimed to be used in a general population rosacea prevalence study.

NCT ID: NCT02292797 Completed - Rosacea Clinical Trials

Assessment of the Rosacea Prevalence in the General Population

RISE
Start date: September 2013
Phase: N/A
Study type: Observational

Multi-centre interventional cross-sectional prevalence study Assessment of the Rosacea Prevalence in the General Population.

NCT ID: NCT02289352 Completed - Rosacea Clinical Trials

Randomized, Double-blind, Multiple-site, Placebo-controlled, Parallel-design Study in Patients With Moderate to Severe Facial Erythema Associated With Rosacea

Start date: July 2014
Phase: Phase 3
Study type: Interventional

A Randomized, Double-Blind, Multiple-Site, Placebo-Controlled, Parallel-Design Study to Evaluate the Safety and Therapeutic Equivalence of Brimonidine Topical Gel, 0.33% (Watson Laboratories, Inc., USA) to Reference Product Mirvaso® (brimonidine) topical gel, 0.33% (Galderma Laboratories, L.P., USA) in Patients with Moderate to Severe Facial Erythema Associated with Rosacea

NCT ID: NCT02270411 Completed - Atopic Dermatitis Clinical Trials

Inflammatory Cells From Various Pathologies

Start date: May 2014
Phase:
Study type: Observational

The objective of this experiment is to develop and validate in vitro methods to isolate inflammatory cells from skin biopsies for quantitative flow cytometry analysis. Real-time polymerase chain reaction (RT-PCR) will also be performed using skin biopsy samples to validate flow cytometry results. Such methods could eventually be used to better understand the pathophysiology and the mechanism of action of various medications in patients with atopic dermatitis, acne rosacea or vulgaris, HS, and systemic sclerosis. In this study, up to 15 healthy volunteers, 50 patients with atopic dermatitis, 15 patients with acne rosacea, 15 patients with psoriasis (to be used as control), 15 patients with acne vulgaris, 10 patients with psoriasis to develop a method of analysis for systemic sclerosis, and 10 patients with HS will be recruited. For the healthy volunteers, atopic dermatitis, psoriasis and HS groups, at least one (1) and a maximum of four (4) skin biopsies (4-5 mm) per subject will be performed. Biopsies will be performed on either the trunk or the limbs, excluding the hands and the feet. At least one (1) and a maximum of three (3) skin biopsies (2-3 mm) per subject will be collected for the acne rosacea and acne vulgaris groups from one or more body location(s) affected by the pathology. For patients with atopic dermatitis, an optional blood draw of up to 10 mL will be collected to measure serum IgE levels. For patients with atopic dermatitis, psoriasis, and HS, an optional blood collection of up to 50 mL will be collected to perform flow cytometry on circulating blood cells to study differences in flow cytometry results between cells extracted from biopsies and circulating cells.

NCT ID: NCT02268474 Completed - Clinical trials for Papulopustular Rosacea

Excel V 532 nm KTP Laser for Treatment of Erythematotelangiectatic Rosacea & Papulopustular Rosacea

Start date: September 2014
Phase: N/A
Study type: Interventional

A single center prospective, randomized, controlled split face study comparing a 532nm KTP laser with a 595nm PDL for the treatment of Erythematotelangiectatic Rosacea and Papulopustular Rosacea. Subjects will receive laser treatments and will be followed at 6 weeks post-final laser treatment.

NCT ID: NCT02249065 Completed - Rosacea Clinical Trials

Mirvaso in Use Study

Start date: September 2014
Phase: Phase 4
Study type: Interventional

This study is designed to: 1. assess the signs and symptoms of rosacea, including erythema, without treatment and during treatment with Mirvaso® gel 2. further characterize lifestyle impact and patient satisfaction with Mirvaso® treatment 3. gain a better understanding of the real-world use of Mirvaso® on the pattern and management of facial erythema of rosacea.

NCT ID: NCT02204254 Completed - Rosacea Clinical Trials

RosaC-RF : Bipolar Radiofrequency vs Doxycycline in Rosacea

Rosac-RF
Start date: March 2014
Phase: N/A
Study type: Interventional

Rosacea is a chronic facial disfiguring dermatosis characterized by different stages like flushing, erythema, telangiectasia and papulo-pustular lesions. Recommended treatments include topical (metronidazole) and systemic (doxycycline) antibiotics with only a suspensive effect. The bipolar radiofrequency (RF) with Elos system (infrared light) is a device emitting an electromagnetic current inducing an increase in temperature when applied on the skin, potentiated by infrared light. The monopolar RF has already been used in rosacea on a small number of cases with positive and prolonged results. RF with Elos system has been evaluated on erythemato-telangiectasic rosacea with encouraging results. Demodex folliculorum (DF) is a long transparent mite which asymptomatically parasitizes pilosebaceous follicle of normal human skin sometimes responsible of inflammatory facial dermatoses. The prevalence and density of DF are increased in rosacea, and DF is suspected to play a role in the pathogenesis of rosacea. DF is sensitive to heat, and the investigators hypothesize that radiofrequency treatment may affect the survival of the mite and should be effective to treat papulopustular rosacea.