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NCT00636597 · ClinicalTrials.gov registry record
A Prospective Evaluation of Same Day Bidirectional Endoscopy for Occult Bleeding
A clinical trial, sponsored by US Department of Veterans Affairs.
- Terminated
- Registry status
- 200
- Enrollment target
NCT00636597: Clinical Trial study, sponsored by US Department of Veterans Affairs.
NCT00636597 is a clinical trial that was terminated before completion, run by US Department of Veterans Affairs. The registered enrollment target is 200 participants. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00636597 was terminated before completion, sponsored by US Department of Veterans Affairs.
- TERMINATED
- Registry status
- 200 participants
- Enrollment target
Study Summary
This study is a prospective evaluation of patients with occult (hidden) GI bleeding without iron deficiency. Such patients usually undergo a diagnostic colonoscopy as a standard of care. The study is aimed to determine any UGI-source of occult bleeding and to correlate UGI symptoms with findings. Therefore, EGD is being offered to such patients as part of research. We proposed to enroll 200 consecutive patients referred to our GI-unit for expedited diagnostic colonoscopy for positive FOBT.
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 200 participants |
| Start Date | 2007-04 |
| Est. Completion | 2011-06 |
Why NCT00636597 stopped before completion
NCT00636597 is an observational study that tracks outcomes without assigning an intervention. The registered 200 participants enrollment target is mid-sized for trials with a published cap.
The record links to 0 conditions, and to 0 interventions.
NCT00636597 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00636597 about?
NCT00636597 is a clinical study titled "A Prospective Evaluation of Same Day Bidirectional Endoscopy for Occult Bleeding". This study is a prospective evaluation of patients with occult (hidden) GI bleeding without iron deficiency. Such patients usually undergo a diagnostic colonoscopy as a standard of care. The study is aimed to determine any UGI-source of occult bleeding and to correlate UGI symptoms with findings. Th...
What is the current status of trial NCT00636597?
This trial is currently terminated. The enrollment target is 200 participants. The study started on 2007-04. Estimated completion is 2011-06.
Who is sponsoring clinical trial NCT00636597?
This trial is sponsored by US Department of Veterans Affairs, which has 632 total clinical trials registered on ClinicalTrials.gov.
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