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NCT00224042 · ClinicalTrials.gov registry record · Phase 4
Effect of Ferrlecit® Versus Oral Iron on Iron Deficient Chronic Kidney Disease (CKD) Patients Receiving Erythropoietic Agents
A Phase 4 study, sponsored by Watson Pharmaceuticals.
- Completed
- Registry status
- Phase 4
- Development phase
- 52
- Enrollment target
NCT00224042 is a Phase 4 study that has completed, run by Watson Pharmaceuticals. The registered enrollment target is 52 participants.
The verdict
NCT00224042, a Phase 4 study, has completed, sponsored by Watson Pharmaceuticals.
- COMPLETED
- Registry status
- Phase 4
- Development phase
- 52 participants
- Enrollment target
Study Summary
This study compares the effect of Ferrlecit® (a form of intravenous iron) to ferrous sulfate (a form of oral iron) in treating anemia and iron deficiency in chronic kidney disease patients who are receiving erythropoietic agents, such as Procrit® and Aranesp®.
Interventions
- DRUG Ferrous sulfate tablets
- DRUG Sodium Ferric Gluconate complex in sucrose
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 52 participants |
| Start Date | 2003-04 |
| Phase | Phase 4 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00224042
The ClinicalTrials.gov registry entry for NCT00224042 describes a study currently listed as completed, categorized as Phase 4. The registered enrollment target is 52 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Watson Pharmaceuticals, which has 28 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which Ferrous sulfate tablets is the first listed.
NCT00224042 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT00224042 about?
NCT00224042 is a clinical study titled "Effect of Ferrlecit® Versus Oral Iron on Iron Deficient Chronic Kidney Disease (CKD) Patients Receiving Erythropoietic Agents". This study compares the effect of Ferrlecit® (a form of intravenous iron) to ferrous sulfate (a form of oral iron) in treating anemia and iron deficiency in chronic kidney disease patients who are receiving erythropoietic agents, such as Procrit® and Aranesp®.
What is the current status of trial NCT00224042?
This trial is currently completed. It is a Phase 4 study. The enrollment target is 52 participants. The study started on 2003-04.
What interventions are being tested in trial NCT00224042?
The interventions under investigation include: Ferrous sulfate tablets (DRUG), Sodium Ferric Gluconate complex in sucrose (DRUG).
Who is sponsoring clinical trial NCT00224042?
This trial is sponsored by Watson Pharmaceuticals, which has 28 total clinical trials registered on ClinicalTrials.gov.
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