Sildenafil for Treatment of Digital Ulcers in Patients With Systemic Sclerosis (Sildenafil)
Primary Purpose
Active Digital Ulcers
Status
Completed
Phase
Phase 2
Locations
Germany
Study Type
Interventional
Intervention
Sildenafil therapy
Sponsored by
About this trial
This is an interventional treatment trial for Active Digital Ulcers focused on measuring digital ulcers,, systemic sclerosis,, sildenafil,, vasoactive therapies
Eligibility Criteria
Inclusion Criteria:
- Digital gangrene, ulcers in patients with severe secondary Raynaud's phenomenon
- Stable therapy with vasoactive drugs, such as calcium channel blockers, angiotensin inhibitors/AT II receptor antagonists or pentoxifyllin 4 weeks before and during the treatment with sildenafil.
- Unchanged immunosuppressive therapy 3 months before treatment with sildenafil
- No effect of prostacyclin treatment, contraindications for prostacyclins, or other reasons excluding this therapy
Exclusion Criteria:
- Therapy with iloprost during the last 4 weeks
- Sympathectomy during the last 4 weeks
- TIA, stroke, myocardial infarction during the last 6 months
- Instable angina pectoris
- Hemorrhagic diathesis, thrombocytic dysfunction, fibromuscular dysplasia
- Microangiopathic hemolytic anaemia
- Azotaemia
- Hypertonus not adjustable with diuretic, clonidine, ACE inhibitors/AT II antagonists, calcium channel blockers)
- Left ventricular ejection fraction< 20%
- Hypotonus < 80/40 mm Hg
- Positive pregnancy test
- History of cancer
- History of gastric/duodenic ulcers without endoscopic proof of complete healing
- Participation in other studies (currently or during the last 4 weeks)
- Abuse of alcohol or other drugs, smoker
- Cardiac failure, use of nitrates
Sites / Locations
- Riemekasten, PD Dr. med.
Arms of the Study
Arm 1
Arm Type
Other
Arm Label
1, active ulcers
Arm Description
sildenafil treatment
Outcomes
Primary Outcome Measures
healing of digital ulcer
Secondary Outcome Measures
Decrease of frequency/duration of Raynaud's attacks (monthly)
Prevention of necroses manifestations
Full Information
NCT ID
NCT00624273
First Posted
February 14, 2008
Last Updated
January 6, 2009
Sponsor
Charite University, Berlin, Germany
1. Study Identification
Unique Protocol Identification Number
NCT00624273
Brief Title
Sildenafil for Treatment of Digital Ulcers in Patients With Systemic Sclerosis
Acronym
Sildenafil
Official Title
Effect of Sildenafil on Digital Ulcers in Systemic Sclerosis
Study Type
Interventional
2. Study Status
Record Verification Date
July 2003
Overall Recruitment Status
Completed
Study Start Date
February 2004 (undefined)
Primary Completion Date
November 2004 (Actual)
Study Completion Date
February 2007 (Actual)
3. Sponsor/Collaborators
Name of the Sponsor
Charite University, Berlin, Germany
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
This is a pilot study analyzing the effect of sildenafil therapy on digital ulcers in systemic sclerosis. We want to analyze ulcer healing by measuring the size of digital ulcers and their count and analyze the effect of sildenafil on angiography.
Detailed Description
INVESTIGATOR: Dr. Gabriela Riemekasten Anke Praast Prof. G. R. Burmester Prof. Falk Hiepe
OBJECTIVES:
Sildenafil is a very potent drug in the treatment of digital ulcers secondary to Raynaud´s phenomenon in patients with connective tissue diseases. Probably, sildenafil has a disease-modifying capability improving different signs of a disturbed regulation of vascular tone in connective tissue diseases. Sildenafil can be used over a long period without significant side effects in scleroderma patients and improves disease severity, life quality, and prognosis of patients with connective tissue diseases and secondary Raynaud's phenomenon.
SUBJECTS and CENTERS:
We want to study 10-15 patients with digital ulcers secondary to connective tissue diseases and which are refractory to other drugs, such as calcium channel blockers or iloprost. In this pilot study, patients are treated only in the Charité University Hospital.
INCLUSION/EXCLUSION CRITERIA
1 . Digital gangrene, ulcers in patients with severe secondary Raynaud's phenomenon
2. Stable therapy with vasoactive drugs, such as calcium channel blockers, angiotensin inhibitors/AT II receptor antagonists or pentoxifyllin 4 weeks before and during the treatment with sildenafil.
3. Unchanged immunosuppressive therapy 3 months before treatment with sildenafil
4. No effect of prostacyclin treatment, contraindications for prostacyclins, or other reasons excluding this therapy
EXCLUSION CRITERIA:
Therapy with iloprost during the last 4 weeks
Sympathectomy during the last 4 weeks
TIA, stroke, myocardial infarction during the last 6 months
Instable angina pectoris
Hemorrhagic diathesis, thrombocytic dysfunction, fibromuscular dysplasia
Microangiopathic hemolytic anaemia
Azotaemia
Hypertonus not adjustable with diuretic, clonidine, ACE inhibitors/AT II antagonists, calcium channel blockers)
Left ventricular ejection fraction< 20%
Hypotonus < 80/40 mm Hg
Positive pregnancy test
History of cancer
History of gastric/duodenic ulcers without endoscopic proof of complete healing
Participation in other studies (currently or during the last 4 weeks)
Abuse of alcohol or other drugs, smoker
Cardiac failure, use of nitrates
STUDY DESIGN:
This is an open prospective pilot study of one centre determining the effect of a 6 month treatment of sildenafil in patients with acral ulcers in secondary Raynaud's phenomenon due to connective tissue diseases.
Drop out criteria's/ final points:
1 . Any change of the immunomodulating or suppressing therapy (e.g., treatment with cyclophosphamide because of an alveolitis; bolus of steroids > 30 mg/d).
2. No response on the healing of ulcers after 4 weeks of treatment with sildenafil 3. Manifestation of new ulcers/necrosis under sildenafil 4. Escalation of medication with an vascular influence (calcium channel blockers, ACE inhibitors/AT II receptor blockers)
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Active Digital Ulcers
Keywords
digital ulcers,, systemic sclerosis,, sildenafil,, vasoactive therapies
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
17 (Actual)
8. Arms, Groups, and Interventions
Arm Title
1, active ulcers
Arm Type
Other
Arm Description
sildenafil treatment
Intervention Type
Drug
Intervention Name(s)
Sildenafil therapy
Other Intervention Name(s)
start at 25 mg
Intervention Description
oral use
Primary Outcome Measure Information:
Title
healing of digital ulcer
Time Frame
6 months
Secondary Outcome Measure Information:
Title
Decrease of frequency/duration of Raynaud's attacks (monthly)
Time Frame
6 months
Title
Prevention of necroses manifestations
Time Frame
6 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Digital gangrene, ulcers in patients with severe secondary Raynaud's phenomenon
Stable therapy with vasoactive drugs, such as calcium channel blockers, angiotensin inhibitors/AT II receptor antagonists or pentoxifyllin 4 weeks before and during the treatment with sildenafil.
Unchanged immunosuppressive therapy 3 months before treatment with sildenafil
No effect of prostacyclin treatment, contraindications for prostacyclins, or other reasons excluding this therapy
Exclusion Criteria:
Therapy with iloprost during the last 4 weeks
Sympathectomy during the last 4 weeks
TIA, stroke, myocardial infarction during the last 6 months
Instable angina pectoris
Hemorrhagic diathesis, thrombocytic dysfunction, fibromuscular dysplasia
Microangiopathic hemolytic anaemia
Azotaemia
Hypertonus not adjustable with diuretic, clonidine, ACE inhibitors/AT II antagonists, calcium channel blockers)
Left ventricular ejection fraction< 20%
Hypotonus < 80/40 mm Hg
Positive pregnancy test
History of cancer
History of gastric/duodenic ulcers without endoscopic proof of complete healing
Participation in other studies (currently or during the last 4 weeks)
Abuse of alcohol or other drugs, smoker
Cardiac failure, use of nitrates
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Dr. Gabriela Riemekasten, MD
Organizational Affiliation
Charité Universitätsklinik Berlin
Official's Role
Principal Investigator
Facility Information:
Facility Name
Riemekasten, PD Dr. med.
City
Berlin
ZIP/Postal Code
10117
Country
Germany
12. IPD Sharing Statement
Learn more about this trial
Sildenafil for Treatment of Digital Ulcers in Patients With Systemic Sclerosis
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