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Iron supplementation in patients with anemia

Adherence to iron supplementation in reproductive-age women with anemia in West Papua, Province, Indonesia

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN96148278
Enrollment
222
Registered
2022-10-25
Start date
2019-10-01
Completion date
Unknown
Last updated
2023-05-01

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

Conditions

Moderate and severe anemia Haematological Disorders

Interventions

Participants are randomised to take one of two oral supplements daily for 30 days. The iron fumarate-folic acid (IF-FA) supplement contains the elemental iron equivalent of 30 mg and 400 µg of folic a
the Medication Adherence Rating Score (MARS) tool
and the participants' perspective on adherence. For biomarker observations, hemoglobin levels are measured pre and post intervention.

Sponsors

Padjadjaran University
Lead Sponsor
Teluk Bintuni General Hospital
Collaborator
Indonesian Ministry for Research, Technology, and Higher Education
Collaborator

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: 1. Moderate and severe anemia 2. Aged between 15–49 years 3. Consented to take part in the study

Exclusion criteria

Exclusion criteria: 1. Did not complete the informed consent 2. Incomplete data collected pre and post session 3. Unable to communicate

Design outcomes

Primary

MeasureTime frame
Hemoglobin level measured using the portable analyzer HemoCue 201 at baseline and 30 days

Secondary

MeasureTime frame
Correlation factors to the success of anemia therapy such as ethnicity, adherence to MARS and pill counting methods, and the type of supplementation, measured at baseline and 30 days

Countries

Indonesia

Outcome results

None listed

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