drugset / Trial / NCT04594070
Daily Versus Alternate Day Iron Supplementation for the Treatment of Iron Deficiency Anemia in Pregnancy
RandomizedParallel-groupOpen-labelTreatment
Summary
The target population for our study is pregnant women in the first or second trimester with a diagnosis of iron deficiency anemia. If a subject is eligible, written consent will be obtained by person to person contact. Eligible participants will be randomized to receive either daily oral iron supplementation or every other day oral iron supplementation.
Timeline
- Start
- 2020-10-27
- Primary completion
- 2024-01-12
- Completion
- 2024-01-12
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Ferrous Sulfate | Diagnostic / imaging agent | 325 mg | Oral |
| Subject | Ferrous Sulfate | Diagnostic / imaging agent | 650 mg | Oral |