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NCT00236977 · ClinicalTrials.gov registry record · Phase 3
Comparison of Safety and Efficacy of Intravenous Iron Versus Oral Iron in Chronic Renal Failure Subjects With Anemia
A Phase 3 study, sponsored by American Regent.
- Completed
- Registry status
- Phase 3
- Development phase
- 182
- Enrollment target
NCT00236977: Completed Phase 3 study, sponsored by American Regent.
NCT00236977 is a Phase 3 study that has completed, run by American Regent. The registered enrollment target is 182 participants, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (76% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00236977, a Phase 3 study, has completed, sponsored by American Regent.
- COMPLETED
- Registry status
- Phase 3
- Development phase
- 182 participants
- Enrollment target
Study Summary
To assess the safety and efficacy of two forms of iron therapy for the treatment of anemia in non-dialysis dependent, chronic renal failure in patients receiving or not receiving erythropoietin.
Interventions
- DRUG Ferrous Sulfate
- DRUG Venofer
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 182 participants |
| Start Date | 2003-08 |
| Est. Completion | 2004-10 |
| Phase | Phase 3 |
What the finished NCT00236977 record still lists
NCT00236977 is an interventional study that assigns participants to a tested intervention. The registered 182 participants enrollment target is mid-sized for trials with a published cap, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (76% lower).
The record links to 0 conditions, and to 2 interventions - of which Ferrous Sulfate is the first listed.
NCT00236977 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00236977 about?
NCT00236977 is a clinical study titled "Comparison of Safety and Efficacy of Intravenous Iron Versus Oral Iron in Chronic Renal Failure Subjects With Anemia". To assess the safety and efficacy of two forms of iron therapy for the treatment of anemia in non-dialysis dependent, chronic renal failure in patients receiving or not receiving erythropoietin.
What is the current status of trial NCT00236977?
This trial is currently completed. It is a Phase 3 study. The enrollment target is 182 participants. The study started on 2003-08. Estimated completion is 2004-10.
What interventions are being tested in trial NCT00236977?
The interventions under investigation include: Ferrous Sulfate (DRUG), Venofer (DRUG).
Who is sponsoring clinical trial NCT00236977?
This trial is sponsored by American Regent, which has 34 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT00236977's enrollment target sits among peer trials
182 1421st of 2000 higher than 579 of 2,000 other Phase 3 trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Phase 3 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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