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NOT YET RECRUITING
NCT07708090
NA

An RCT Study Between WHO and RCOG Based Practices

Sponsor: Sana Nadeem Qasir

View on ClinicalTrials.gov

Summary

We are 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, we will compare these two methods to see which one is more helpful and suitable for mothers. Your participation will help us improve care for women after childbirth in the future. Taking part is your choice, and all your information will be kept private.

Official title: A Randomized Controlled Trial Comparing WHO- and RCOG-Based Practices for Routine Iron Supplementation in Postpartum Women With Normal Hemoglobin Level

Key Details

Gender

FEMALE

Age Range

18 Years - 40 Years

Study Type

INTERVENTIONAL

Enrollment

100

Start Date

2026-09-01

Completion Date

2026-12-20

Last Updated

2026-07-16

Healthy Volunteers

No

Interventions

DRUG

Iron Polymaltose Complex with folic acid

Participants in the intervention group will receive drug Polymalt F (iron polymaltose complex with folic acid), one tablet orally once daily for 6 weeks after delivery. The purpose of this intervention is to evaluate whether routine iron supplementation helps prevent postpartum anemia in women with normal hemoglobin levels.

Locations (1)

Regional headquarters hospital chilas

Chilas, Gilgitbaltistan, Pakistan