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NCT00395993 · ClinicalTrials.gov registry record · Phase 3
Comparison of the Safety and Efficacy of Intravenous Iron Versus Oral Iron in the Treatment of Anemia Secondary to Heavy Uterine Bleeding
A Phase 3 study, sponsored by American Regent.
- Completed
- Registry status
- Phase 3
- Development phase
- 456
- Enrollment target
NCT00395993: Completed Phase 3 study, sponsored by American Regent.
NCT00395993 is a Phase 3 study that has completed, run by American Regent. The registered enrollment target is 456 participants, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (41% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00395993, a Phase 3 study, has completed, sponsored by American Regent.
- COMPLETED
- Registry status
- Phase 3
- Development phase
- 456 participants
- Enrollment target
Study Summary
This study compares of the safety and efficacy of intravenous iron vs oral iron in the treatment of anemia secondary to heavy uterine bleeding
Interventions
- DRUG Ferric Carboxymaltose (FCM)
- DRUG Ferrous Sulfate tablets
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 456 participants |
| Start Date | 2005-05 |
| Est. Completion | 2006-06 |
| Phase | Phase 3 |
What the finished NCT00395993 record still lists
NCT00395993 is an interventional study that assigns participants to a tested intervention. The registered 456 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 (41% lower).
The record links to 0 conditions, and to 2 interventions - of which Ferric Carboxymaltose (FCM) is the first listed.
NCT00395993 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00395993 about?
NCT00395993 is a clinical study titled "Comparison of the Safety and Efficacy of Intravenous Iron Versus Oral Iron in the Treatment of Anemia Secondary to Heavy Uterine Bleeding". This study compares of the safety and efficacy of intravenous iron vs oral iron in the treatment of anemia secondary to heavy uterine bleeding
What is the current status of trial NCT00395993?
This trial is currently completed. It is a Phase 3 study. The enrollment target is 456 participants. The study started on 2005-05. Estimated completion is 2006-06.
What interventions are being tested in trial NCT00395993?
The interventions under investigation include: Ferric Carboxymaltose (FCM) (DRUG), Ferrous Sulfate tablets (DRUG).
Who is sponsoring clinical trial NCT00395993?
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 NCT00395993's enrollment target sits among peer trials
456 827th of 2000 higher than 1,172 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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