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Prognostic Influence of Light Rheography Measurement of Patients With Secondary Raynaud Syndrome With Ulcers on Hands (Anti-Vasospasm)

Primary Purpose

Raynaud's Phenomenon, Skin Necrosis

Status
Unknown status
Phase
Not Applicable
Locations
Germany
Study Type
Interventional
Intervention
Tracleer
Prostavasin
Sponsored by
Christoph Hehrlein
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Raynaud's Phenomenon focused on measuring Morbus Raynaud, Ulcera Hands, Toes, Vasospastic disorder, Raynaud's phenomenon

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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)

Sites / Locations

  • University FreiburgRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Placebo Comparator

Active Comparator

Arm Label

Prostavasin

Prostavasin + Bosentan

Arm Description

Outcomes

Primary Outcome Measures

Quantification of the blood flow before, during and after the medical therapy
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.

Secondary Outcome Measures

Emerge of new ulcers
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.

Full Information

First Posted
June 16, 2011
Last Updated
December 12, 2014
Sponsor
Christoph Hehrlein
Collaborators
Actelion
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1. Study Identification

Unique Protocol Identification Number
NCT01378845
Brief Title
Prognostic Influence of Light Rheography Measurement of Patients With Secondary Raynaud Syndrome With Ulcers on Hands
Acronym
Anti-Vasospasm
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
Study Type
Interventional

2. Study Status

Record Verification Date
December 2014
Overall Recruitment Status
Unknown status
Study Start Date
July 2011 (undefined)
Primary Completion Date
June 2015 (Anticipated)
Study Completion Date
September 2015 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Christoph Hehrlein
Collaborators
Actelion

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this study is to evaluate the prognostic influence of light rheography measurement at the fingertips from subjects with secundary Raynaud syndrome.
Detailed Description
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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Raynaud's Phenomenon, Skin Necrosis
Keywords
Morbus Raynaud, Ulcera Hands, Toes, Vasospastic disorder, Raynaud's phenomenon

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
30 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Prostavasin
Arm Type
Placebo Comparator
Arm Title
Prostavasin + Bosentan
Arm Type
Active Comparator
Intervention Type
Drug
Intervention Name(s)
Tracleer
Other Intervention Name(s)
Bosentan
Intervention Description
14 days 62,5 mg Bosentan p.o 140 days 125 mg Bosentan p.o
Intervention Type
Drug
Intervention Name(s)
Prostavasin
Other Intervention Name(s)
Aprostadil
Intervention Description
Prostavasin 60 µg i.v, 5 days per week for 2 weeks
Primary Outcome Measure Information:
Title
Quantification of the blood flow before, during and after the medical therapy
Description
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.
Time Frame
24 weeks
Secondary Outcome Measure Information:
Title
Emerge of new ulcers
Description
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.
Time Frame
> 24 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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)
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Christoph Hehrlein, Prof. Dr. med.
Phone
+49 761 270 77090
Email
christoph.hehrlein@uniklinik-freiburg.de
First Name & Middle Initial & Last Name or Official Title & Degree
Mark Kerber, Dr. med.
Phone
+49 761 270 36920
Email
mark.kerber@uniklinik-freiburg.de
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Mark Kerber, Dr. med.
Organizational Affiliation
Universitätsklinik Freiburg
Official's Role
Principal Investigator
Facility Information:
Facility Name
University Freiburg
City
Freiburg
State/Province
Baden Württemberg
ZIP/Postal Code
79106
Country
Germany
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Mark Kerber, MD
Email
mark.kerber@uniklinik-freiburg.de
First Name & Middle Initial & Last Name & Degree
christoph Hehrlein, MD
Email
christoph.hehrlein@uniklinik-freiburg.de

12. IPD Sharing Statement

Citations:
Citation
-Distler O, Gay S. [Scleroderma]. Internist (Berl) 2010; 51(1):30-38. -Mouthon L, Mestre-Stanislas C, Berezne A et al. Impact of digital ulcers on disability and health-related quality of life in systemic sclerosis. Ann Rheum Dis 2010; 69(1):214-217. -Denton C, Krieg T, Guillevin L. The burden of complications in patients with digital ulcers (DU) and systemic sclerosis (SSc): Preliminary findings from the DUO-Registry. 2009: 273. -Korn JH, Mayes M, Matucci CM et al. Digital ulcers in systemic sclerosis: prevention by treatment with bosentan, an oral endothelin receptor antagonist. Arthritis Rheum 2004; 50(12):3985-3993. -Block JA, Sequeira W. Raynaud's phenomenon. Lancet 2001; 357(9273):2042-2048.
Results Reference
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Citation
-Sunderkotter C, Herrgott I, Bruckner C et al. Comparison of patients with and without digital ulcers in systemic sclerosis: detection of possible risk factors. Br J Dermatol 2009; 160(4):835-843. -Muller-Ladner U. Akrale Ischämiesyndrome: vom Raynaud-Syndrom zur systemischen Sklerose. Bremen/London/Boston: UNI-MED Verlag AG, 2009 -Arab A, Kuemmerer K, Wang J et al. Oxygenated perfluorochemicals improve cell survival during reoxygenation by pacifying mitochondrial activity. J Pharmacol Exp Ther 2008; 325(2):417-424. -Pope J, Fenlon D, Thompson A et al. Iloprost and cisaprost for Raynaud's phenomenon in progressive systemic sclerosis. Cochrane Database Syst Rev 2000;(2):CD000953. -Kawald A, Burmester GR, Huscher D et al. Low versus high-dose iloprost therapy over 21 days in patients with secondary Raynaud's phenomenon and systemic sclerosis: a randomized, open, single-center study. J Rheumatol 2008; 35(9):1830-1837. -Kowal-Bielecka O, Landewe R, Avouac J et al. EULAR recommendations for the treatment of systemic sclerosis: a report from the EULAR Scleroderma Trials and Research group (EUSTAR). Ann Rheum Dis 2009; 68(5):620-628. -Sunderkotter C, Riemekasten G. [Raynaud phenomenon in dermatology:Part 2:therapy]. Hautarzt 2006; 57(10):927-938. -Ludwig M. Angiologie in Klinik und Praxis. 1 ed. Stuttgart: Thieme Verlag, 1998; 1-334.
Results Reference
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Prognostic Influence of Light Rheography Measurement of Patients With Secondary Raynaud Syndrome With Ulcers on Hands

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