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NCT06366698 · ClinicalTrials.gov registry record · Phase 3
Intravenous Iron Versus Oral Iron for the Treatment of Iron Deficiency Anemia
A Phase 3 study of Iron Deficiency Anemia of Pregnancy, sponsored by Arrowhead Regional Medical Center.
- Recruiting
- Registry status
- Phase 3
- Development phase
- 900
- Enrollment target
- 1
- Study location
NCT06366698 is a Phase 3 study of Iron Deficiency Anemia of Pregnancy that is actively recruiting participants, run by Arrowhead Regional Medical Center. The registered enrollment target is 900 participants. The trial reports 1 study location across 1 state.
The verdict
NCT06366698, a Phase 3 study of Iron Deficiency Anemia of Pregnancy, is actively recruiting participants, sponsored by Arrowhead Regional Medical Center.
- RECRUITING
- Registry status
- Phase 3
- Development phase
- 900 participants
- Enrollment target
- 1
- Study location
Study Summary
This study aims to assess whether administering intravenous iron early in pregnancy, compared to standard oral iron treatment, can enhance hemoglobin levels before delivery and reduce the need for blood transfusions in patients with iron deficiency anemia. Patients diagnosed with iron deficiency anemia were randomly assigned to receive either oral or intravenous iron. Before treatment initiation, patients completed a symptom questionnaire baseline hemoglobin, and ferritin levels were measured. Follow-up visits occurred four weeks later and at 24 to 28 weeks gestation, involving reassessment of symptoms, laboratory testing, and monitoring of treatment adherence. Final hemoglobin levels were determined before delivery, and data on the need for blood transfusion at delivery were recorded.
Conditions Studied
Interventions
- DRUG Venofer 200 MG Per 10 ML Injection
- DRUG Ferrous sulfate
Study Locations (1)
California
- Arrowhead Regional Medical Center - Colton
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 900 participants |
| Start Date | 2023-11-21 |
| Est. Completion | 2025-12-30 |
| Phase | Phase 3 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06366698
The ClinicalTrials.gov registry entry for NCT06366698 describes a study currently listed as recruiting, categorized as Phase 3. The registered enrollment target is 900 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Arrowhead Regional Medical Center, which has 13 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Iron Deficiency Anemia of Pregnancy appearing as the primary indexed condition, and to 2 interventions - of which Venofer 200 MG Per 10 ML Injection is the first listed.
NCT06366698 reports 1 study location spanning 1 distinct geographic area - top geographies include California.
Frequently Asked Questions
What is clinical trial NCT06366698 about?
NCT06366698 is a clinical study titled "Intravenous Iron Versus Oral Iron for the Treatment of Iron Deficiency Anemia". This study aims to assess whether administering intravenous iron early in pregnancy, compared to standard oral iron treatment, can enhance hemoglobin levels before delivery and reduce the need for blood transfusions in patients with iron deficiency anemia. Patients diagnosed with iron deficiency ane...
What is the current status of trial NCT06366698?
This trial is currently recruiting. It is a Phase 3 study. The enrollment target is 900 participants. The study started on 2023-11-21. Estimated completion is 2025-12-30.
What conditions does trial NCT06366698 study?
This clinical trial studies the following conditions: Iron Deficiency Anemia of Pregnancy.
What interventions are being tested in trial NCT06366698?
The interventions under investigation include: Venofer 200 MG Per 10 ML Injection (DRUG), Ferrous sulfate (DRUG).
Who is sponsoring clinical trial NCT06366698?
This trial is sponsored by Arrowhead Regional Medical Center, which has 13 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06366698 being conducted?
This trial has 1 study location across California. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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