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Raynaud's Disease clinical trials

View clinical trials related to Raynaud's Disease.

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NCT ID: NCT02683408 Completed - Raynaud's Disease Clinical Trials

Diosmiplex (Vasculera®) in Primary and Secondary Raynaud's Phenomenon

Start date: February 2016
Phase: N/A
Study type: Interventional

Diosmiplex is a product marketed for the management of diseases due to venous and microvascular dysfunction. Raynaud's phenomenon is a disorder of characterized by spasm of small arteries and impaired microvascular flow. This study will examine the effects of diosmiplex on the frequency and severity of Raynaud's episodes in susceptible people.

NCT ID: NCT02615964 Enrolling by invitation - Raynaud's Disease Clinical Trials

Nova Cold Hands Raynaud's Disorder, a Disease Which Results in Decreased Blood Flow to the Hands and Feet.

Start date: May 2015
Phase: N/A
Study type: Observational

Patients presenting to UIC rheumatology clinic with Raynaud's disorder and scleroderma will be asked to participate. 10 hands of patients with both Raynaud's disorder and scleroderma will be studied. This research study is being done to better understand Raynaud's disease and to assess the role of blood flow measurement in diagnosing the disorder, specifically, through data collected by an MRI procedure called NOVA FLOW. NOVA is a blood flow measurement software system owned by the study's sponsor, VasSol, Inc.

NCT ID: NCT02396238 Completed - Systemic Sclerosis Clinical Trials

Scleroderma Treatment With Celution Processed Adipose Derived Regenerative Cells (STAR)

STAR
Start date: May 15, 2015
Phase: N/A
Study type: Interventional

The primary objective of this study is to assess the safety and efficacy of the Celution Device in the processing of an autologous graft consisting of adipose derived regenerative cells (ADRCs) in the treatment of hand dysfunction due to scleroderma.

NCT ID: NCT01309802 Completed - Raynaud's Disease Clinical Trials

A Two-Part Study of BOTOX® Therapy for Ischemic Digits

Start date: May 2011
Phase: Phase 2
Study type: Interventional

Treating patients with Raynaud's phenomenon who have chronic pain and ulcerations is extremely challenging. Published reports and our previous work support our hypothesis that symptomatic patients experience relief of pain and healing of ulcerations with minimal adverse effects when treated with botulinum toxin type A (Btx-A) injections for Raynaud's phenomenon. The proposed study is the first clinical trial and prospective study designed to document whether or not 1) Btx-A injection relieves pain in a patient's hand affected with Raynaud's disease better than a placebo within 28 days of injection, and 2) Btx-A injection relieves pain associated with Raynaud's disease for longer than 28 days, improving patients' quality of life. Through this study we intend to further determine the effect of injected Btx-A on relieving chronic pain and ulcerations to the ischemic hand while characterizing the patients for whom this treatment is most effective.

NCT ID: NCT01090492 Completed - Clinical trials for Peripheral Vascular Disease

PF-00489791 For The Treatment Of Raynaud's

Start date: August 4, 2010
Phase: Phase 2
Study type: Interventional

The investigators propose that once daily administration of PF-00489791, a phosphodiesterase inhibitor, will reduce vasospasm and improve symptoms and signs associated with Primary and Secondary Raynaud's Phenomenon.

NCT ID: NCT00577304 Active, not recruiting - Raynaud's Disease Clinical Trials

A Study of a Topical Form of Nitroglycerin and Placebo in the Treatment and Prevention of Raynaud's Phenomenon

Start date: December 2007
Phase: Phase 3
Study type: Interventional

The purpose of this research study is to test the safety, tolerability, and effectiveness of Topical AmphiMatrix with Nitroglycerin (MQX0503) to relieve Raynaud's symptoms and increase blood flow to the fingers.

NCT ID: NCT00528242 Completed - Raynaud's Disease Clinical Trials

Safety, Tolerability, and Pharmacodynamic Profile of Oral 2101 in Secondary Raynaud's Disease

Start date: June 2007
Phase: Phase 2
Study type: Interventional

To investigate the severity of secondary Raynaud's disease-related attacks during the 14 days 2101 dosing period.

NCT ID: NCT00480753 Completed - Raynaud's Disease Clinical Trials

Dose Response Study of a Topical Formulation of Nitroglycerin for the Treatment of Raynaud's Phenomenon

Start date: May 2007
Phase: Phase 2
Study type: Interventional

The purpose of this clinical study is to determine the response to two different dosage strengths of a topical nitroglycerin gel in patients with Raynaud's Phenomenon. Patient fingers will be monitored for changes in blood flow and skin temperature. Symptoms of pain, tingling and numbness will also be monitored.

NCT ID: NCT00419419 Completed - Autoimmune Diseases Clinical Trials

Phase III Study of a Topical Gel Formulation for Treatment and Prevention of Raynaud's Phenomenon

Start date: December 2006
Phase: Phase 3
Study type: Interventional

The purpose of this research study is to test the safety, tolerability, and effectiveness of Topical AmphiMatrix with Nitroglycerin (MQX-503) to relieve Raynaud's symptoms and increase blood flow to the fingers.

NCT ID: NCT00378521 Completed - Raynaud's Disease Clinical Trials

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

Start date: July 2006
Phase: Phase 2
Study type: Interventional

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.