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Rosacea clinical trials

View clinical trials related to Rosacea.

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NCT ID: NCT02774590 Completed - Acne Vulgaris Clinical Trials

Timolol for the Treatment of Acne and Rosacea

Start date: March 2016
Phase: Phase 1
Study type: Interventional

This research is being done to determine the safety and tolerability of timolol in the treatment of acne and rosacea. The investigators will also look for specific biomolecular changes in acne or rosacea skin when it is exposed to timolol. Timolol is approved by the Food and Drug Administration (FDA) for the treatment of glaucoma. In dermatology, it has been used as a treatment to decrease the size of vascular (blood vessel) malformations in infant skin. Timolol is not approved for use in acne or rosacea and its use in this study is investigational. Many people with rosacea have telangiectasias which are small, red dilated blood vessels on the skin. They also suffer from flushing and acne-like lesions. Better treatments than those currently available are desired. Acne vulgaris, or acne, is another chronic inflammatory and very common skin disease that affects about 8 out of 10 young adults and adolescents. Signs of acne include papules and blackheads that are often called primary lesions because they represent an active form of the disease. There are also secondary lesions that can form later; they are known as acne scars

NCT ID: NCT02749786 Completed - Rosacea Clinical Trials

Genetic Basis of Rosacea Study (Control)

Start date: January 21, 2016
Phase: N/A
Study type: Interventional

Rosacea is a common disease characterized by inflammation and vascular abnormalities of the facial skin and ocular surface. It it considered to be a syndrome encompassing various combinations of cutaneous signs including flushing, erythema, telangiectasia, papules, edema, ocular lesions, and rhinophyma. The exact etiology of cutaneous rosacea is unknown but is characterized by persistent vasodilation, increased vascular permeability, and vascular hyper-reactivity of the microcirculation of the central part of the face. The purpose of this study is to develop gene expression profiles of papulopustular rosacea compared to those of normal skin. The investigator hopes to better understand the abnormal gene functions that might contribute to this condition. This understanding may lead to the development of additional and better treatments for rosacea.

NCT ID: NCT02637232 Completed - Rosacea Clinical Trials

Mirvaso® Utilisation and Patient Satisfaction Evaluation (MUSE)

MUSE
Start date: October 2015
Phase:
Study type: Observational

The aim of the study is to evaluate the level of satisfaction among patients to whom Mirvaso® / Onreltea TM (trade mark) is prescribed.

NCT ID: NCT02616250 Completed - Rosacea Clinical Trials

MirvasO Soolantra Association In the Treatment of Moderate to Severe rosaCea.

MOSAIC
Start date: December 2015
Phase: Phase 4
Study type: Interventional

The main objective of this study is to evaluate the efficacy of Ivermectin 1% cream (IVM) associated with Brimonidine 0.33% gel (Br) compared with the association of their respective vehicles in the treatment of moderate to severe rosacea.

NCT ID: NCT02602470 Completed - Rosacea Clinical Trials

Preferences & Treatment Satisfaction Drivers in Rosacea Patients

Start date: January 8, 2015
Phase:
Study type: Observational

To survey patients with rosacea about their rosacea treatment preferences as well as to assess potential drivers of rosacea treatment satisfaction.

NCT ID: NCT02601963 Completed - Rosacea Clinical Trials

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

EMIRA
Start date: September 2015
Phase: Phase 2
Study type: Interventional

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.

NCT ID: NCT02583009 Completed - Rosacea Clinical Trials

A Study to Evaluate the Safety and Efficacy of PAC-14028 Cream in Rosacea

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

This clinical study is to determine the optimum dose of PAC-14028 cream in a therapeutic confirmatory clinical study by evaluating the safety and therapeutic equivalence of PAC-14028 cream 0.1%, 0.3% and 1.0% in patients with rosacea.

NCT ID: NCT02576860 Completed - Rosacea Clinical Trials

Study to Evaluate the Safety and Efficacy of a Once-Daily CLS001 Topical Gel Versus Vehicle

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

This study evaluates the safety and efficacy of once-daily application of CLS001 topical gel compared to vehicle gel in subjects with severe papulopustular rosacea.

NCT ID: NCT02576847 Completed - Rosacea Clinical Trials

Study to Evaluate the Long-term Safety of a Once-Daily Omiganan Topical Gel

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

This study evaluates the long-term safety of once-daily application of Omiganan topical gel in subjects with severe papulopustular rosacea.

NCT ID: NCT02547441 Completed - Rosacea Clinical Trials

Study to Evaluate the Safety and Efficacy of a Once-Daily CLS001 Topical Gel Versus Vehicle

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

This study evaluates the safety and efficacy of once-daily application of CLS001 topical gel compared to vehicle gel in subjects with severe papulopustular rosacea.