CompletedNot applicableNCT00697385
The Use of Cyclokapron for Treatment and Management of Women With Bleeding Disorders
Studying Hemophilia
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
- Mary M. Gooley Hemophilia Center
- Principal Investigator
- Peter A Kouides, MDMary M. Gooley Hemophilia Center
- Intervention
- Cyclokapron(drug)
- Enrollment
- 13 enrolled
- Eligibility
- 8-60 years · FEMALE
- Timeline
- 2003 – 2008
Study locations (1)
- Mary M. Gooley Hemophilia Center, Rochester, New York, United States
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.
Open NCT00697385 on ClinicalTrials.govOther trials for Hemophilia
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