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Rosacea clinical trials

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NCT ID: NCT04889703 Withdrawn - Rosacea Clinical Trials

A Pilot Study Testing the Effects of Chemical Peels in Patients With Rosacea

Start date: December 2022
Phase: N/A
Study type: Interventional

The study is a prospective, randomized, one-site therapeutic trial of 15% trichloroacetic acid (TCA) and 30% salicylic acid peels for rosacea. Two peels will be applied topically 4 weeks apart, and the study will end in 12 weeks. Endpoints include adverse affects within the first 8 weeks and responses, which will be measured by Investigator Global Assessment (IGA), a Rosacea Clinical Scorecard, and number of papular plus pustular lesions assessed every 4 weeks up to 12 weeks with high resolution photographs. Treatment Dosage and administration Study Drugs: 1. Trichloroacetic acid peel (15%) will be applied topically to the face for 2 treatments at 4 week intervals. 2. Salicylic acid peel (30%) will be applied topically to the face for 2 treatments at 4 week intervals. Duration of treatment: two single applications 4 weeks apart. Endpoint: 12 weeks after first chemical peel treatment Outcome measures: - independent objective reviewer scoring of matched photographs before and after treatment - number of papular and pustular lesions before and after treatment - rosacea-specific patient quality of life survey responses before and after treatment - Adverse effects such as peeling, redness, scaling, crusting, blister formation, and hyperpigmentation will be assessed clinical

NCT ID: NCT04839549 Withdrawn - Ocular Rosacea Clinical Trials

Efficacy and Safety of Dextenza Compared to Topical Fluorometholone in Patients With Ocular Rosacea

Start date: June 6, 2020
Phase: Phase 4
Study type: Interventional

To determine patient preference and treatment outcomes with an intracanalicular dexamethasone (0.4mg) insert compared to a standard steroid drop regimen in the contralateral eye for the treatment of ocular rosacea.

NCT ID: NCT03883945 Withdrawn - Clinical trials for Papulopustular Rosacea

A Safety and Efficacy Study to Evaluate Rosacea

Start date: July 2021
Phase: Phase 1/Phase 2
Study type: Interventional

To evaluate the safety, efficacy, and pharmacokinetic profile of ascending concentrations of the study medication compared with vehicle in subjects with rosacea.

NCT ID: NCT03053700 Withdrawn - Rosacea Clinical Trials

Intense Pulsed Light as an Adjunctive to Bromonidine for the Treatment of Rosacea

Start date: December 1, 2018
Phase: Phase 4
Study type: Interventional

This is an interventional and prospective study. The study is designed to evaluate the additional benefits of a combination of IPL treatment and local application of Bromonide 0.33% gel in the treatment of erythematotelangiectatic (ETR) and papulopustular (PPR).

NCT ID: NCT02735681 Withdrawn - Clinical trials for Meibomian Gland Dysfunction

Effect of Meibomian Gland Probing on Ocular Surface in Ocular Rosacea

Start date: February 1, 2017
Phase: N/A
Study type: Interventional

Meibomian glands (MG) are modified sebaceous glands associated with the tarsus (collagenous structural component) of the upper and lower eyelids. Meibomian glands produce lipid-based secretions which are an integral and stabilizing part of the tear film. In blepharitis and ocular rosacea (two known causes of obstructive meibomian gland dysfunction (o-MGD), inflammation of the lid margins causes blockage of the meibomian gland orifices, changes in glandular secretions, and dropout of the glands themselves. This limits the production, secretion, and quality of meibum. With less oil in the tear film, the aqueous portion of tears is not stable and evaporates quickly which leads to dry eye.

NCT ID: NCT01359228 Withdrawn - Rosacea Clinical Trials

Rifaximin Treatment of Papulopustular Rosacea

Start date: April 2013
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine the effects of rifaximin on skin symptoms in patients with rosacea by double-blinded, placebo-controlled, crossover study.