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NCT Number: NCT07657455

Daily Versus Alternate-Day Oral Iron Therapy for Anemia in Second-Trimester Pregnancy

This randomized controlled trial compares daily versus alternate-day oral iron supplementation in pregnant women with iron deficiency anemia during the second trimester. The study evaluates changes in hemoglobin and serum ferritin, treatment adherence, and gastrointestinal side effects to inform more patient-centered, physiologically aligned dosing strategies.

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Key information

Age range

18 year–40 year

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

Pakistan Air Force (PAF) Hospital Islamabad

Islamabad, Pakistan

About this study

Iron deficiency anemia is the leading cause of anemia in pregnancy. Although daily oral iron is standard first-line therapy, it is frequently associated with gastrointestinal side effects and poor adherence. Because hepcidin rises after an iron dose and remains elevated for 24 to 48 hours, daily dosing may reduce fractional absorption; alternate-day dosing allows hepcidin to fall between doses, potentially improving absorption and tolerance.

This single-center, prospective, randomized, parallel-group trial will recruit pregnant women (13 to 27 weeks gestation) with hemoglobin below 11 g/dL and serum ferritin below 30 ng/mL from the antenatal clinic at PAF Teaching Hospital, Islamabad. Eligible, consenting participants will be randomized 1:1 to daily ferrous sulfate (one 325 mg tablet, approximately 65 mg elemental iron, once daily) or alternate-day ferrous sulfate (two 325 mg tablets, approximately 130 mg elemental iron, every other day) for four weeks.

The primary outcome is change in hemoglobin from baseline to Week 4. Secondary outcomes are change in serum ferritin, treatment adherence (proportion taking at least 80 percent of doses, by pill count and diary), and the frequency and severity of gastrointestinal side effects. Outcome assessors (laboratory personnel) are blinded to allocation; participant blinding is not feasible given the differing dosing schedules. Planned enrollment is 184 participants (92 per group), giving 90 percent power to detect a 0.40 g/dL difference in hemoglobin change at a two-sided alpha of 0.05, assuming a standard deviation of 0.83 g/dL.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Aged 18 to 40 years
  • Pregnant women in the second trimester (13 to 27 weeks gestation)
  • Hemoglobin below 11 g/dL with serum ferritin below 30 ng/mL
  • Singleton pregnancy

Exclusion criteria

  • Known congenital or acquired hemoglobin disorders (e.g., thalassemia, hemoglobinopathies)
  • Chronic diseases affecting hemoglobin levels (e.g., chronic kidney disease, inflammatory disorders)
  • Bleeding disorders or a history of frequent blood loss
  • Gastrointestinal conditions impairing nutrient absorption (e.g., celiac disease or other malabsorption syndromes)
  • Currently receiving parenteral iron
  • Requiring blood transfusion

Treatment and study plan

Ferrous Sulfate

Drug

Oral ferrous sulfate 325 mg tablets (approximately 65 mg elemental iron per tablet) administered for four weeks according to the assigned dosing schedule. All participants receive standardized counseling on administration, diet, side effects, and adherence, and are issued a dose diary.

Primary outcomes

  1. Change in hemoglobin from baseline to Week 4

    Time frame: Baseline and Week 4

    Mean within-participant change in hemoglobin concentration (g/dL), measured at baseline and at Week 4, compared between the daily and alternate-day arms.

Secondary outcomes

  1. Change in serum ferritin from baseline to Week 4

    Time frame: Baseline and Week 4

    Mean within-participant change in serum ferritin concentration (ng/mL) from baseline to Week 4, compared between groups.

  2. Treatment adherence

    Time frame: Through Week 4

    Proportion of participants taking at least 80 percent of prescribed doses, determined by pill count cross-checked against patient dose diaries.

  3. Frequency of gastrointestinal side effects

    Time frame: Through Week 4

    Proportion of participants reporting any gastrointestinal side effect (nausea, vomiting, constipation, metallic taste, or abdominal discomfort) recorded using a structured checklist.

  4. Severity of gastrointestinal side effects

    Time frame: Through Week 4

    Severity of reported gastrointestinal side effects graded as mild, moderate, or severe on a structured checklist.

Study contacts

Contact information is provided by the study sponsor or research team.

Ammara Suleman

CONTACT

[email protected]

+92 321 5279502

Sponsors and collaborators

Lead sponsor

Pakistan Air Force (PAF) Hospital Islamabad

Other

Registry information

Official study title

Daily Versus Alternate-Day Oral Iron Therapy for Anemia Correction in Second-Trimester Pregnant Patients: A Randomized Controlled Trial

Important dates

Study start
2026
Primary completion
2026
Study completion
2027
First posted
Jun 18, 2026
Registry last updated
Jun 18, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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