An RCT Study Between WHO and RCOG Based Practices

Starting soon · Not applicable

Conditions studied: Postpartum Anemia

In brief

Investigator is doing this study to understand the best way to give iron supplements to mothers after delivery who already have a normal blood level (hemoglobin). Some guidelines recommend one approach, while others recommend a different approach. In this study, investigator will compare these two methods to see which one is more helpful and suitable for mothers. Participants participation will help us improve care for women after childbirth in the future. Taking part is participants choice, and all participants information will be kept private.

Key facts

Study ID

NCT07708090

Run by

Sana Nadeem Qasir

People needed

100

Starts

2026-09-01

Expected to finish

2026-12-20

Last updated by the study team

2026-08-05

Who can join

Age: 18 and older, up to 40. Sex: female. Healthy volunteers: not accepted.

You may qualify if…

• Women aged 18-40 years
• Single Term Vaginal delivery
• Hemoglobin ≥10.5 g/dL at 24hour of delivery
• Willing for follow-up

You may not qualify if…

• Postpartum hemorrhage
• Hemoglobin <10.5 g/dL
• Blood transfusion received
• Known hematological disease
• Chronic liver or kidney disease
• Cesarian section

Where it is running

• Regional headquarters hospital chilas — Chilas, Gilgitbaltistan, Pakistan

Full record on ClinicalTrials.gov

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