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Spots Global Cancer Trial Database for Dose Response Study of a Topical Gel for the Treatment of Raynaud's Phenomenon

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Trial Identification

Brief Title: Dose Response Study of a Topical Gel for the Treatment of Raynaud's Phenomenon

Official Title: Phase II Dose Response Study of a Topical Gel Formulation of Nitroglycerin, MQX-503, in the Treatment of Raynaud's Phenomenon

Study ID: NCT00378521

Interventions

MQX-503

Study Description

Brief Summary: The Purpose of this study is to determine the response to two different strengths of a topical gel containing nitroglycerin in patients with Raynaud's disease.

Detailed Description: The Purpose of this clinical study is to determine, in a controlled fashion, the response to two dosage strengths of a topical gel formulation of Nitroglycerin, MQX-503, in the determination of changes in finger blood flow and skin temperature in the fingers of patients with moderate to severe primary Raynaud's phenomenon and with Raynaud's phenomenon secondary to autoimmune diseases, such as scleroderma. The dosage strength response in the treatment of the symptoms (pain, tingling, numbness) will also be monitored.

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Rainier Clinical Research, Renton, Washington, United States

Contact Details

Name: Leslie Klaff, MD

Affiliation: Rainier Clinical Research

Role: PRINCIPAL_INVESTIGATOR

Useful links and downloads for this trial

Clinicaltrials.gov

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