TerminatedPhase 2NCT00622687
Effect of Different Iloprost Doses on Symptoms in Systemic Sclerosis
Studying Diffuse cutaneous systemic sclerosis
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Charite University, Berlin, Germany
- Principal Investigator
- Gabriela Riemekasten, MDCharite University, Berlin, Germany
- Intervention
- iloprost(drug)
- Enrollment
- 50 enrolled
- Eligibility
- 18-80 years · All sexes
- Timeline
- 1997 – 2007
Study locations (1)
- Charrité Universitätsmedizin, Berlin, State of Berlin, Germany
Collaborators
Schering-Plough
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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