Iron Deficiency and Scoliosis Study

This study is looking at whether giving iron supplements before surgery can help teenagers and young adults (ages 10-26) with scoliosis who are having spinal fusion surgery. Participants will either receive oral ferrous sulfate (an iron supplement) or an oral placebo tablet (a pill with no active medicine). We want to see if iron supplementation can reduce the need for blood transfusions during or after surgery, and potentially improve how well patients recover physically and mentally. To join, you need to have scoliosis or kyphosis, be able to swallow a tablet, have surgery planned in 6-24 weeks, and have low iron levels (serum ferritin less than or equal to 25 µg/L). The study is currently recruiting about 275 participants.

Study design
This is a randomized controlled trial, meaning participants will be randomly assigned to receive either the iron supplement or a placebo. The study aims to enroll 275 participants.
What's involved
Not specified in the trial record.
Compensation
Not stated in the trial record.
Follow-up
The primary outcome, incidence of perioperative RBC transfusion, will be measured at 4 to 30 days after surgery.

AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.

NCT06042699

Kids With Iron Deficiency and Scoliosis

Recruiting
NAAges 10–26InterventionalPrevention
Columbia University
~275 participants
Updated 2026-06-26 on ClinicalTrials.gov
What's tested:Oral ferrous sulfateOral placebo tablet

At a glance

Recruiting sites
1 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Incidence of perioperative RBC transfusion in iron deficient scoliosis patients undergoing spinal fusion
Measured over 4 to 30 days
Adolescent Idiopathic Scoliosis
Neuromuscular Scoliosis
Perioperative/Postoperative Complications
Iron Deficiencies
Anemia
Spinal Fusion
Postoperative Cognitive Dysfunction

NCT06042699

Where you'd take part

This study runs at 1 site. They're the same protocol — you choose where, and that choice sets who your contact draft is addressed to.

  • Columbia University Medical Center

    New York, New Yorkstudy coordinator listed

    Recruiting

Sites open and close at different times, so the status above is per site — it can differ from the study's overall status.

  • Lisa D Eisler, MD · PRINCIPAL_INVESTIGATOR · Columbia University

Opens a ready-to-send draft in your own email app — review before sending.

  • Incidence of perioperative RBC transfusion in iron deficient scoliosis patients undergoing spinal fusion4 to 30 days

    The patients that received a red blood cell transfusion either during procedure or postoperatively during t surgical hospitalization will be tallied.