Pilot Study of Epoetin Alfa for Patients Having Abdominal or Pelvic Surgery for Cancer
Completed · Phase 1 · Has a placebo group
Conditions studied: Anemia
In brief
This pilot study is looking at how well epoetin alfa, given in the immediate post-operative period, works in reducing anemia and the need for transfusions.
Key facts
- Study ID
- NCT00294203
- Run by
- University of Florida
- People needed
- 40
- Starts
- 2006-02-01
- Expected to finish
- 2008-12-01
- Last updated by the study team
- 2014-04-15
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Patients undergoing esophagectomy, gastrectomy, partial pancreatectomy, hepatic resection, or low anterior resection of rectum for malignancy
- Patients with hemoglobin greater than 8 and less than 11 g/dL on post-operative day #1.
You may not qualify if…
- Patients receiving red blood cell transfusion within the first twelve hours post-operatively.
- Patients receiving epoetin-stimulating proteins within 30 days prior to the operation.
Where it is running
- Shands Hospital at the University of Florida — Gainesville, Florida, United States
- University of Florida Shands Cancer Center — Gainesville, Florida, United States
Full record on ClinicalTrials.gov
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