Prognostic Influence of Light Rheography Measurement of Patients With Secundary Raynaud Syndrome With Ulcers on Hands (Anti-Vasospasm)
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Purpose
The purpose of this study is to evaluate the prognostic influence of light rheography measurement at the fingertips from subjects with secundary Raynaud syndrome.
| Condition | Intervention |
|---|---|
|
Raynaud's Phenomenon Skin Necrosis |
Drug: Tracleer Drug: Prostavasin |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Safety/Efficacy Study Intervention Model: Parallel Assignment Masking: Open Label Primary Purpose: Prevention |
| Official Title: | Monocenter, IIT, Open Controlled and Prospectiv Study to Define the Prognostic Influence of Light Rheography Measurement of Patients With Secundary Raynaud Syndrome With Ulcers at Fingertips Throughout the Medicinal Therapy |
- Quantification of the blood flow before, during and after the medical therapy [ Time Frame: 24 weeks ] [ Designated as safety issue: No ]The primary objective of this study is defined by the dynamics of the (post)capillary blood flow before (baseline value) and 12 weeks after treatment, measured by means of the LRR. In doing so, the therapeutic effect, in terms of the change in (post)capillary blood flow after treatment compared to baseline value, is to be quantitatively determined.
- Emerge of new ulcers [ Time Frame: > 24 weeks ] [ Designated as safety issue: No ]Additionally, it is to be examined if new DUs emerge after 24 weeks or not. The prospects for recovery of the DU will be investigated by means of visual analogue scale (VAS), photo-documentation, and D-LRR after 2, 6, 12, and 24 weeks of medicinal therapy. Furthermore, as mentioned above, the change in the HIF-1alpha gene expression before (baseline value) and 6 weeks after treatment is to be analyzed.
| Estimated Enrollment: | 30 |
| Study Start Date: | July 2011 |
| Estimated Study Completion Date: | June 2013 |
| Estimated Primary Completion Date: | December 2012 (Final data collection date for primary outcome measure) |
-
Drug: Tracleer
- Tracleer
- Bosentan
Digital Ulcers (DU) belong to one of the most prevalent complications of systemic scleroses, leading in course to considerable impairment in everyday and professional life. The aetiology of the emergence of DU in patients with systemic scleroses (SSc) is complex, whereas the disease itself is primarily characterized by a vasculopathy of the small arterial vessels. In the course of the disease this chronic infection leads to fibrotic intimal hyperplasia, adventitial fibrosis, and thus to a significant lumen narrowing. So far, a number of independent risk factors have been identified, such as male gender, chronic infections of the esophagus, pulmonary-arterial hypertension, evidence of specific antibodies (e.g. anti-Scl70) in the blood, or the a previous manifestation of a Raynoud Syndrom.
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- Subjects with Limited or diffuse systemic sclerosis/scleroderma with at least one ulcera at fingertip
- Age > 18 Years
- Weight > 40 Kg
Exclusion Criteria:
- Sympathectomy
- Ulcers due to other condition (PVD, DM, Thromboangiitis obliterans etc.)
- Antibiotic concomitant medication
- Therapy with Prostanoids within the last 4 weeks
- Previous Bosentan therapy
- Severe liver and renal insufficiency(creatinin >2.0 mg/dl;AST/ALT > 3X UNL)
- severe cardiac- pulmonal diseases
- Untreated or therapy refractory Hypertension
- Noncompliance
- Pregnancy or nursing (Pregnancy test required)
Contacts and Locations| Contact: Christoph Hehrlein, Prof. Dr. med. | +49 761 270 77090 | christoph.hehrlein@uniklinik-freiburg.de |
| Contact: Mark Kerber, Dr. med. | +49 761 270 36920 | mark.kerber@uniklinik-freiburg.de |
| Germany | |
| University Freiburg | Recruiting |
| Freiburg, Baden Württemberg, Germany, 79106 | |
| Contact: Mark Kerber, MD mark.kerber@uniklinik-freiburg.de | |
| Contact: christoph Hehrlein, MD christoph.hehrlein@uniklinik-freiburg.de | |
| Principal Investigator: | Mark Kerber, Dr. med. | Universitätsklinik Freiburg |
More Information
No publications provided
| Responsible Party: | Christoph Hehrlein, Professor Dr. med., University of Freiburg |
| ClinicalTrials.gov Identifier: | NCT01378845 History of Changes |
| Other Study ID Numbers: | 2011-002127-17 |
| Study First Received: | June 16, 2011 |
| Last Updated: | December 13, 2011 |
| Health Authority: | Germany: Ethics Commission |
Keywords provided by University of Freiburg:
|
Morbus Raynaud Ulcera Hands, Toes Vasospastic disorder Raynaud's phenomenon |
Additional relevant MeSH terms:
|
Raynaud Disease Necrosis Pathologic Processes Peripheral Vascular Diseases Vascular Diseases Cardiovascular Diseases Alprostadil Bosentan Platelet Aggregation Inhibitors |
Hematologic Agents Therapeutic Uses Pharmacologic Actions Vasodilator Agents Cardiovascular Agents Fibrinolytic Agents Fibrin Modulating Agents Molecular Mechanisms of Pharmacological Action Antihypertensive Agents |
ClinicalTrials.gov processed this record on May 22, 2013