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Raynaud Disease clinical trials

View clinical trials related to Raynaud Disease.

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NCT ID: NCT02680509 Completed - Raynauds Clinical Trials

Single-port Thoracoscopic Sympathicotomy for Treatment of Raynaud's Phenomenon, a Feasibility Study

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

The goal is to investigate the effect of a single-port R3 sympathicotomy on microvascular circulation in the affected fingers. This effect is analysed by performing cooling plethysmography and nailfold capillary microscopy bilaterally, following a unilateral, single-port thoracoscopic sympathicotomy.

NCT ID: NCT02642146 Terminated - Systemic Sclerosis Clinical Trials

Treatment of Digital Ulcers in Korean Patients With Systemic Sclerosis: a Prospective Cohort Study

Start date: January 2015
Phase:
Study type: Observational [Patient Registry]

This study evaluates the efficacy and safety of routine medical treatments of digital ulcers in patients with systemic sclerosis in a prospective cohort study.

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: NCT02583789 Completed - Clinical trials for Raynaud's Phenomenon

Assess Efficacy of of Oral Treprostinil in Patients With Symptomatic Primary or Secondary Raynaud's Phenomenon

Start date: May 2016
Phase: Early Phase 1
Study type: Interventional

This study represents the first trial to assess the efficacy of oral treprostinil therapy in patients with symptomatic primary or secondary Raynaud's Phenomenon (RP) resistant to vasodilatory therapy. The study will be randomized 1:1 UT-15C to placebo. The design is a crossover study and all subjects will be randomized to receive oral treprostinil sustained release tablets or matching placebo for 12 weeks and then crossover for 12 weeks. All subjects will be exposed for 12 weeks of treatment with oral UT-15C during the study.

NCT ID: NCT02506062 Completed - Raynaud Disease Clinical Trials

A Trial of Ischemic Preconditioning in Raynaud's Phenomenon (RP)

Start date: July 2015
Phase: N/A
Study type: Interventional

This trial will test the efficacy of brief periods of controlled limb ischemia (remote ischemic preconditioning, RIPC) as an effective treatment of patients with Raynaud's Phenomenon (RP).The hypothesis of this trial is that due to its vasoprotective effects, RIPC would be more effective than placebo in the treatment of both primary and secondary RP, as defined by decreased frequency, duration, and severity of attacks. This trial was also designed to monitor the tolerance of RIPC in a rheumatologic population. Patients will not be required to stop any current treatment for RP.

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: NCT02374320 Terminated - Clinical trials for Peripheral Vascular Disease

Exparel as a Nerve Block for Severe Hand Pain

Start date: November 2014
Phase: Phase 2/Phase 3
Study type: Interventional

The purpose of this study is to investigate whether the use of the study drug (Exparel) is safe and effective for treating circulation problems and pain in the hand or fingers.

NCT ID: NCT02356809 Not yet recruiting - Clinical trials for Secondary Raynaud's Phenomenon

Safety and Efficacy Study of Gene Therapy Drug (Neovasculgen) to Treat Secondary Raynaud's Phenomenon

Start date: March 2015
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this study is to determine whether pl-vegf165 (Neovasculgen) is effective in the treatment of digital ulcers related to secondary Raynaud's phenomenon associated with systemic scleroderma

NCT ID: NCT02298777 Recruiting - Vascular Disease Clinical Trials

Metabolomic Analysis of Systemic Sclerosis

SCLEROMICS
Start date: December 2014
Phase:
Study type: Observational

Currently investigators do not have diagnostic and prognostic markers for SSc which almost always starts with a vascular disease (Raynaud's disease) isolated for several years. The primary purpose is to highlight discriminating metabolic profiles depending on the characteristics of the disease, allowing early diagnosis of SSc at the onset of vascular lesions, by comparing the profiles of SSc beginners (<3 years) to established forms (> 3 years). Secondary purposes: - Prognosis: to study the metabolomics profile of SSc when a visceral complication occurs - Diagnosis: to compare the metabolomics profile of SSc to undifferentiated connective tissue disease (UCDT), Raynaud's disease (RD), vascular disease (VD) and healthy controls - Exploratory: to compare the metabolomics profile of blood, urine and skin of SSc patients

NCT ID: NCT02260557 Completed - Clinical trials for Raynaud's Phenomenon Secondary to Systemic Sclerosis

Effects of Selexipag in Adults With Raynaud's Phenomenon Secondary to Systemic Sclerosis

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

The primary objective of the study is to determine the activity of selexipag on Raynaud attack frequency in subjects with Raynaud's Phenomenon (RP) secondary to Systemic Sclerosis (SSc).