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Rosacea clinical trials

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NCT ID: NCT02095158 Completed - Rosacea Clinical Trials

A Long-Term Safety and Efficacy Study AGN-19920 in Patients With Persistent Erythema Associated With Rosacea

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

This study will evaluate the long-term safety and efficacy of oxymetazoline hydrogen chloride (HCL) Cream 1.0% (AGN-199201) in patients with persistent erythema associated with rosacea.

NCT ID: NCT02075671 Completed - Rosacea Clinical Trials

Photodynamic Therapy for Papulopustular Rosacea

Start date: April 24, 2014
Phase: Phase 4
Study type: Interventional

Rosacea is a chronic inflammatory disorder that is characterized by severe flushing (transient erythema), non-transient erythema, papules, pustules, and telangiectasia. Topical therapy is not always effective in treating symptoms of rosacea. Furthermore, rapid recurrence is common following the use of systemic antibiotics, resulting in the chronic use of these medications to control the disease. Although the exact pathogenesis of rosacea is unknown, treatment for this condition has been investigated based on its similarity to acne and photodamaged skin. Case reports have shown promising results in rosacea patients treated with methyl aminolevulinate photodynamic therapy (MAL - PDT). Other than a case report which observed significant improvement of papules, pustules, erythema, and flushing following 5 - aminolevulinic acid photodynamic therapy (ALA-PDT) treatment of a patient with rosacea, the role of ALA-PDT in the treatment of rosacea has not been reported. We have designed a pilot study investigating the efficacy of ALA-PDT in treating papulopustular rosacea. The objectives of the study are as follows: Primary objective: 1. To evaluate improvement of the inflammatory lesions (papules, pustules, nodules), erythema, and telangiectasia of rosacea as assessed by the Investigator's Global Assessment (IGA). 2. To evaluate improvement of the inflammatory lesions (papules, pustules, nodules) of rosacea as assessed by the Inflammatory Lesion Investigator's Global Assessment (ILIGA). Secondary objectives: 3. To evaluate improvement of rosacea associated erythema as assessed by the Clinical Erythema Assessment (CEA) scale. 4. To evaluate improvement of the inflammatory lesions (papules, pustules, nodules) of rosacea as measured by a difference in inflammatory lesion count. 5. To evaluate improvement of rosacea as assessed by the Patient Overall Assessment Scale.

NCT ID: NCT02066051 Completed - Dry Eye Syndrome Clinical Trials

IPL and Meibomian Gland Expression to Treat Ocular Rosacea Ocular GVHD

Start date: October 2013
Phase: N/A
Study type: Interventional

The purpose of this study was to see if Intense Pulsed Light (IPL) can be used safely and effectively to help treat dry eyes from ocular rosacea after chronic graft-versus-host disease (GVHD). Current treatment options for this disease are limited.

NCT ID: NCT02052999 Completed - Clinical trials for Papulopustular Rosacea

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

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

The objective of this study is to determine the efficacy and safety of PAC-14028 1% cream of Amorepacific Corporation in patients with erythema-telangiectatic or papulopustular rosacea

NCT ID: NCT02036229 Recruiting - Rosacea Clinical Trials

Topical 0.5% Ivermectin Cream for Treatment of Demodicidosis

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

The purpose of this study is to determine whether 0.5% ivermectin cream is effective in the treatment of demodicidosis (including papulopustular rosacea)

NCT ID: NCT02028286 Completed - Clinical trials for Papulopustular Rosacea

A 21 Day Pharmacokinetics Study in Papulopustular Rosacea

Start date: January 2014
Phase: Phase 1
Study type: Interventional

The purpose of this study is to characterize the pharmacokinetics of once daily topical gel and confirm that steady state conditions are reached under maximal use conditions following 3 weeks of daily applications.

NCT ID: NCT01993446 Completed - Rosacea Clinical Trials

A Safety and Efficacy Study of DRM02 in Subjects With Rosacea

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

The purpose of this study is to determine whether DRM02 is safe and effective in the treatment of rosacea when applied twice daily for 6 weeks.

NCT ID: NCT01933464 Completed - Clinical trials for Papulopustular Rosacea

An Analysis of the Effect of Topical Cromolyn Sodium on Rosacea-associated Erythema

Start date: August 2013
Phase: Phase 1/Phase 2
Study type: Interventional

This study is designed to investigate whether topical application of a cromolyn sodium solution is able to decrease the facial redness seen in patients with papulopustular rosacea. Previous work in the lab of Dr. Di Nardo on mice has suggested that cromolyn may be able to have this effect. The study will enroll a total of 10 patients. 5 will randomly be assigned to receive the cromolyn sodium solution, and the other 5 will be randomly assigned to receive the placebo solution. All participants will be instructed to apply their assigned solution twice daily to their face. Patients will return to the clinic 3, 6, and 8 weeks after the distribution of the solutions to measure the efficacy of their assigned solution.

NCT ID: NCT01931644 Completed - Breast Cancer Clinical Trials

At-Home Research Study for Patients With Autoimmune, Inflammatory, Genetic, Hematological, Infectious, Neurological, CNS, Oncological, Respiratory, Metabolic Conditions

Start date: July 2013
Phase:
Study type: Observational

We are the missing link in clinical trials, connecting patients and researchers seamlessly and conveniently using a mobile health platform to advance medical research. We make it easy for patients to contribute to research for medical conditions that matter most to them, regardless of their location or ability to travel.

NCT ID: NCT01885000 Completed - Rosacea Clinical Trials

Patient-Reported Outcome Of Facial Erythema (PROOF)

PROOF
Start date: July 1, 2013
Phase: Phase 3
Study type: Interventional

The purpose of the study is to evaluate the patient-reported outcomes (feedbacks of patients)of a new drug for the treatment of erythema of rosacea (central facial redness). The feedback of patients receiving the active drug will be compared to the feedback of patients receiving the placebo.