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NCT00450177 · ClinicalTrials.gov registry record · Phase 2
Efficacy of Enteral Iron Supplementation in Critical Illness
A Phase 2 study, sponsored by Weill Medical College of Cornell University.
- Completed
- Registry status
- Phase 2
- Development phase
- 200
- Enrollment target
NCT00450177: Completed Phase 2 study, sponsored by Weill Medical College of Cornell University.
NCT00450177 is a Phase 2 study that has completed, run by Weill Medical College of Cornell University. The registered enrollment target is 200 participants, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (50% higher). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00450177, a Phase 2 study, has completed, sponsored by Weill Medical College of Cornell University.
- COMPLETED
- Registry status
- Phase 2
- Development phase
- 200 participants
- Enrollment target
Study Summary
The purpose of this study is to investigate the efficacy of enteral iron supplementation for improving anemia, decreasing the risk of blood transfusion, and decreasing mortality in patients who are hospitalized in the intensive care unit. This study will also address any relationship between enteral iron supplementation and risk of infection.
Interventions
- DRUG Ferrous Sulfate
- DRUG Placebo Oral Tablet
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 200 participants |
| Start Date | 2006-01 |
| Est. Completion | 2008-01 |
| Phase | Phase 2 |
What the finished NCT00450177 record still lists
NCT00450177 is an interventional study that assigns participants to a tested intervention. The registered 200 participants enrollment target is mid-sized for trials with a published cap, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (50% higher).
The record links to 0 conditions, and to 2 interventions - of which Ferrous Sulfate is the first listed.
NCT00450177 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00450177 about?
NCT00450177 is a clinical study titled "Efficacy of Enteral Iron Supplementation in Critical Illness". The purpose of this study is to investigate the efficacy of enteral iron supplementation for improving anemia, decreasing the risk of blood transfusion, and decreasing mortality in patients who are hospitalized in the intensive care unit. This study will also address any relationship between enteral...
What is the current status of trial NCT00450177?
This trial is currently completed. It is a Phase 2 study. The enrollment target is 200 participants. The study started on 2006-01. Estimated completion is 2008-01.
What interventions are being tested in trial NCT00450177?
The interventions under investigation include: Ferrous Sulfate (DRUG), Placebo Oral Tablet (DRUG).
Who is sponsoring clinical trial NCT00450177?
This trial is sponsored by Weill Medical College of Cornell University, which has 701 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT00450177's enrollment target sits among peer trials
200 304th of 2000 higher than 1,652 of 2,000 other Phase 2 trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Phase 2 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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