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NCT06622551Completed

Different Efficacy of IFA Supplementation Among Obese and Non-obese Women

The Study of Association Between Obesity and Iron Deficiency Anaemia in Nonpregnant Indonesian Women

Source: ClinicalTrials.gov · Last updated 11 Jun 2026

Brief summary (registry, in English)

This clinical trial aims to learn if there is a relationship between OWT/OB and IDA in nonpregnant women of reproductive age and its impact on iron supplementation. The main questions it aims to answer are: * Is there any independent association between overweight/obesity and iron deficiency anemia in nonpregnant women after controlling for potential confounding factors? * Does the effect of iron supplementation on iron status vary between overweight/obese and normal-weight nonpregnant women (as measured by multiple iron biomarkers)? Researchers will compare several biomarkers between the case and control groups after the intervention is given for 90 days. Participants will: * Visit the research center before the intervention given and after 90 days * Take daily iron-folic acid supplements for 90 days * Keep a diary of their supplement's intake

Status (registry)
Completed
Study type
Interventional
Enrollment
165 (actual)
First submitted
26 Sept 2024
Start date
1 Aug 2024
Primary completion date
31 Dec 2024
Lead sponsor
Griffith University
Diseases
Obesity
NCT number
NCT06622551

What you commit to

  • Study type: Interventional
  • Participants enrolled: 165
  • From 1 Aug 2024 to the primary completion date, 31 Dec 2024
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Self-reported specific diseases that need diet modification (i.e., type 1 diabetes, kidney disease, autoimmune disease, etc.)
  • Self-report of significant medical conditions (e.g., diabetes mellitus, disorders of the liver \[including hemochromatosis\] and kidney, autoimmune or metabolic diseases, and malignancy\] or use of medications that may influence weight, iron, or inflammatory status; pregnancy or lactation; vegetarianism; zinc supplementation; smoking habit.

Other

  • BMI \<18.5 kg/m2

Who the study is looking for

  • Nonpregnant, nonlactating women aged 19 - 29 years
  • Never been married and pregnant.
  • Having no menstrual abnormality (amenorrhea, polymenorrhea, etc.)
  • Able to read and write in Bahasa Indonesia
  • Not undergoing body mass reduction or on any particular weight loss diet

Age in the registry: 20 years to 29 years · Sex: Female · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Nutrition Laboratory, Faculty of Public Health Universitas Airlangga
Coordinator of this site? Confirm its status
SurabayaIndonesiaUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.