Extra daily iron after sleeve gastrectomy to prevent anemia

Prophylactic Oral Iron Supplementation for the Prevention of Iron Deficiency Anemia After Sleeve Gastrectomy: A Prospective Comparative Cohort Study

Cairo University · NCT07397572

This study tests whether taking an extra daily iron pill plus a multivitamin prevents iron deficiency anemia in adults during the six months after sleeve gastrectomy compared with taking a multivitamin alone.

Quick facts

Study typeObservational
Enrollment66 (estimated)
Ages18 Years to 65 Years
SexAll
SponsorCairo University (other)
Locations1 site (Cairo, Al-Manial Cairo)
Trial IDNCT07397572 on ClinicalTrials.gov

What this trial studies

This prospective observational cohort study at Kasr Al-Ainy Hospital, Cairo University, compares two routine post-operative supplement strategies in adults undergoing primary laparoscopic sleeve gastrectomy. One cohort receives prophylactic daily elemental iron (Ferrodep 60 mg) in addition to a standard multivitamin, while the other cohort receives only a standard multivitamin (Centrum Silver), with cohort assignment determined by the treating surgical unit's usual practice. Iron indices and anemia status are measured before surgery and at 3 and 6 months post-operatively as part of routine care, and health and quality-of-life information are collected during follow-up visits. The primary outcome is the incidence of iron deficiency anemia within six months after surgery.

Who should consider this trial

Good fit: Adults aged 18 to 65 scheduled for primary laparoscopic sleeve gastrectomy who can provide informed consent and attend the 3- and 6-month follow-up visits are the intended participants.

Not a fit: Patients with prior major gastrointestinal surgery, known malabsorptive conditions, or other non-iron anemias (e.g., thalassemia, B12/folate deficiency) are unlikely to benefit from this comparison.

Why it matters

Potential benefit: If successful, routine prophylactic oral iron could reduce rates of post-operative iron deficiency anemia and improve quality of life after sleeve gastrectomy.

How similar studies have performed: Prior work shows iron deficiency is common after sleeve gastrectomy, but direct comparative data on routine prophylactic iron versus multivitamin-only approaches are limited and inconclusive.

Eligibility criteria

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Adults aged 18 to 65 years scheduled to undergo primary laparoscopic sleeve gastrectomy (LSG).
* Capable of understanding and providing written informed consent for participation.
* Able and willing to commit to the 6-month post-operative follow-up schedule at the bariatric clinic.

Exclusion Criteria:

* Prior history of major gastrointestinal surgery (e.g., bowel resection, gastrectomy) that could independently affect iron absorption.
* Pre-existing malabsorptive conditions (e.g., inflammatory bowel disease, celiac disease).
* Diagnosis of other known forms of anemia (e.g., thalassemia, vitamin B12/folate deficiency, anemia of chronic disease) that would confound the diagnosis of iron deficiency anemia (IDA).
* Any condition that, in the investigator's judgment, would interfere with full participation in the study or pose a significant risk.

Where this trial is running

Cairo, Al-Manial Cairo

Study contacts

How to participate

  1. Review the eligibility criteria above with your treating physician.
  2. Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
  3. Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.

View on ClinicalTrials.gov →

Conditions: Iron Deficiency Anemia, Obesity, Sleeve Gastrectomy, Laparoscopic Sleeve Gastrectomy, Bariatric Surgery, Iron Supplementation, Multivitamin, Morbid Obesity

Last reviewed 2026-05-15 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.