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Sildenafil for Treatment of Digital Ulcers in Patients With Systemic Sclerosis

Effect of Sildenafil on Digital Ulcers in Systemic Sclerosis

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00624273
Acronym
Sildenafil
Enrollment
17
Registered
2008-02-27
Start date
2004-02-29
Completion date
2007-02-28
Last updated
2009-01-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Active Digital Ulcers

Keywords

digital ulcers,, systemic sclerosis,, sildenafil,, vasoactive therapies

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: 1. Therapy with iloprost during the last 4 weeks 2. Sympathectomy during the last 4 weeks 3. TIA, stroke, myocardial infarction during the last 6 months 4. Instable angina pectoris 5. Hemorrhagic diathesis, thrombocytic dysfunction, fibromuscular dysplasia 6. Microangiopathic hemolytic anaemia 7. Azotaemia 8. Hypertonus not adjustable with diuretic, clonidine, ACE inhibitors/AT II antagonists, calcium channel blockers) 9. Left ventricular ejection fraction\< 20% 10. Hypotonus \< 80/40 mm Hg 11. Positive pregnancy test 12. History of cancer 13. History of gastric/duodenic ulcers without endoscopic proof of complete healing 14. Participation in other studies (currently or during the last 4 weeks) 15. Abuse of alcohol or other drugs, smoker 16. 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)

Interventions

oral use

Sponsors

Charite University, Berlin, Germany
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion 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

1. Therapy with iloprost during the last 4 weeks 2. Sympathectomy during the last 4 weeks 3. TIA, stroke, myocardial infarction during the last 6 months 4. Instable angina pectoris 5. Hemorrhagic diathesis, thrombocytic dysfunction, fibromuscular dysplasia 6. Microangiopathic hemolytic anaemia 7. Azotaemia 8. Hypertonus not adjustable with diuretic, clonidine, ACE inhibitors/AT II antagonists, calcium channel blockers) 9. Left ventricular ejection fraction\< 20% 10. Hypotonus \< 80/40 mm Hg 11. Positive pregnancy test 12. History of cancer 13. History of gastric/duodenic ulcers without endoscopic proof of complete healing 14. Participation in other studies (currently or during the last 4 weeks) 15. Abuse of alcohol or other drugs, smoker 16. Cardiac failure, use of nitrates

Design outcomes

Primary

MeasureTime frame
healing of digital ulcer6 months

Secondary

MeasureTime frame
Decrease of frequency/duration of Raynaud's attacks (monthly)6 months
Prevention of necroses manifestations6 months

Countries

Germany

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026