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A Study Comparing Weekly (60 mg) and Twice-Weekly (30 mg) Iron Tablets in Healthy Adolescent Girls to Improve Regular Intake and Reduce Side Effects

Impact of Dose Optimization on Compliance to Iron Folic Acid Supplementation among Adolescent Girls: Open labelled Non-Randomized Controlled Trial at Ahmedabad District, Gujarat - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/12/099617
Enrollment
400
Registered
2025-12-22
Start date
Unknown
Completion date
Unknown
Last updated
2026-01-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Intervention1: Biweekly Iron Folic Acid with 30 mg iron: IFA tablets having 30 mg iron and 250 mcg folic acid will be administered twice weekly Control Intervention1: Weekly Iron Folic Acid with 60 mg

Sponsors

State Health System Resource Center, Gujarat
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Adolescent girls in their middle or late adolescent age (14 to 19 years), who herself or whose parents are ready to give written informed assent /consent to participate in the study.

Exclusion criteria

Exclusion criteria: 1.Adolescent girl who will be anemic at the time of baseline assessment. 2.Adolescent girl who is already on Iron therapy for treatment of anemia. 3.Adolescent girl who is diagnosed with hemoglobinopathies (Sickle cell anemia, Thalassemia major/minor). 4. Adolescent girl who is currently having any kind of systemic illness (Tuberculosis, Diabetes, Hypertension, Thyroid disorders etc.) which requires treatment.

Design outcomes

Primary

MeasureTime frame
Compliance to Iron and Folic Acid (IFA) supplementation, measured as Proportion of prescribed IFA tablets consumed over the study period, assessed by pill count and/or self-reported intake, compared between weekly 60 mg and twice-weekly 30 mg regimens.Timepoint: End of intervention period, 6 months

Secondary

MeasureTime frame
Frequency and type of self-reported side effectsTimepoint: During intervention period;Hemoglobin levelTimepoint: Baseline and end of intervention

Countries

India

Contacts

Public ContactDr Venu Shah

GCS Medical College, Ahmedabad

drvenushah@gmail.com07966048351

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026