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Completed

NCT Number: NCT00624273

Sildenafil for Treatment of Digital Ulcers in Patients With Systemic Sclerosis

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.

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Key information

Age range

18 year–80 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Riemekasten, PD Dr. med.

Berlin, State of Berlin, 10117, Germany

About this study

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

  • 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

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).

  • 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)

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Sildenafil therapy

Drug

oral use

Other names: start at 25 mg

Primary outcomes

  1. healing of digital ulcer

    Time frame: 6 months

Secondary outcomes

  1. Decrease of frequency/duration of Raynaud's attacks (monthly)

    Time frame: 6 months

  2. Prevention of necroses manifestations

    Time frame: 6 months

Sponsors and collaborators

Lead sponsor

Charite University, Berlin, Germany

Other

Registry information

Official study title

Effect of Sildenafil on Digital Ulcers in Systemic Sclerosis

Acronym: Sildenafil

Important dates

Study start
2004
Primary completion
2004
Study completion
2007
First posted
Feb 27, 2008
Registry last updated
Jan 7, 2009

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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