CompletedEarly Phase 1NCT02117115
Abdominal CT to Predict the Risk of Acute Graft-versus-Host Disease Following Allogeneic Hematopoietic Stem Cell Transplantation
Studying Myelodysplastic/myeloproliferative disease
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
- Washington University School of Medicine
- Principal Investigator
- Amanda Cashen, M.D., MDWashington University School of Medicine
- Intervention
- Dynamic contrast-enhanced computed tomography(radiation)
- Enrollment
- 21 enrolled
- Eligibility
- 20-60 years · All sexes
- Timeline
- 2014 – 2015
Study locations (1)
- Washington University School of Medicine, St Louis, Missouri, 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.
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