CTRI/2020/02/023125
Not yet recruiting
Phase 4
Efficacy, Safety and Acceptability of Intravenous Versus Oral Iron Therapy in Postpartum Anemia - A Randomised Controlled Trial
Department of Obstetrics And Gynecology0 sites0 target enrollmentTBD
Overview
- Phase
- Phase 4
- Intervention
- Not specified
- Conditions
- Not specified
- Sponsor
- Department of Obstetrics And Gynecology
- Status
- Not yet recruiting
- Last Updated
- 4 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Patients with Hemoglobin between 8\-10gm/dl, 36\-48 hours after delivery.
- •Group A will be treated with Intravenous Iron .
- •Group B will be treated with Tablet Iron.
Exclusion Criteria
- •Peripartum Blood Transfusion
- •Intolerance To Iron Derivatives
- •Clotting disorders
- •Patients with Anemia other than that caused by blood loss secondary to delivery and iron deficiency anemia.
Outcomes
Primary Outcomes
Not specified
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