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NCT06042699 · ClinicalTrials.gov registry record · NA

Kids With Iron Deficiency and Scoliosis

A NA study of Anemia and Spinal Fusion, sponsored by Columbia University.

Recruiting
Registry status
NA
Development phase
275
Enrollment target
1
Study location

NCT06042699 is a NA study of Anemia and Spinal Fusion that is actively recruiting participants, run by Columbia University. The registered enrollment target is 275 participants, below the 424-participant average among 72 other Anemia trials with a reported enrollment target (35% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT06042699, a NA study of Anemia and Spinal Fusion, is actively recruiting participants, sponsored by Columbia University.

RECRUITING
Registry status
NA
Development phase
275 participants
Enrollment target
1
Study location

Study Summary

This study is a randomized controlled trial of preoperative oral iron supplementation, to identify whether iron deficiency is a modifiable risk factor for adverse surgical outcomes such as red blood cell transfusion and diminished postoperative cognitive and physical capacity in adolescents undergoing scoliosis surgery. Research Question(s)/Hypothesis(es): Primary * Iron supplementation will reduce the incidence of perioperative RBC transfusion in iron deficient scoliosis patients undergoing spinal fusion. Secondary * Iron supplementation will reduce postoperative neurocognitive functional declines in iron deficient scoliosis patients undergoing spinal fusion. * Iron supplementation will improve patient-reported physical functioning in iron deficient scoliosis patients undergoing spinal fusion.

Interventions

  • DIETARY_SUPPLEMENT Oral ferrous sulfate
  • DIETARY_SUPPLEMENT Oral placebo tablet

Study Locations (1)

New York

  • Columbia University Medical Center - New York

Trial Details

FieldValue
Enrollment Target 275 participants
Start Date 2024-01-11
Est. Completion 2028-02-01
Phase NA

Sponsor

Columbia University

958 total trials

What the Registry Record Tells You About NCT06042699

The ClinicalTrials.gov registry entry for NCT06042699 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 275 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 424-participant average among 72 other Anemia trials with a reported enrollment target (35% lower). The listed sponsor is Columbia University, which has 958 total studies on file at ClinicalTrials.gov.

The record links to 7 conditions, with Anemia appearing as the primary indexed condition, and to 2 interventions - of which Oral ferrous sulfate is the first listed.

NCT06042699 reports 1 study location spanning 1 distinct geographic area - top geographies include New York.

Frequently Asked Questions

What is clinical trial NCT06042699 about?

NCT06042699 is a clinical study titled "Kids With Iron Deficiency and Scoliosis". This study is a randomized controlled trial of preoperative oral iron supplementation, to identify whether iron deficiency is a modifiable risk factor for adverse surgical outcomes such as red blood cell transfusion and diminished postoperative cognitive and physical capacity in adolescents undergoi...

What is the current status of trial NCT06042699?

This trial is currently recruiting. It is a NA study. The enrollment target is 275 participants. The study started on 2024-01-11. Estimated completion is 2028-02-01.

What conditions does trial NCT06042699 study?

This clinical trial studies the following conditions: Anemia, Spinal Fusion, Perioperative/Postoperative Complications, Adolescent Idiopathic Scoliosis, Postoperative Cognitive Dysfunction.

What interventions are being tested in trial NCT06042699?

The interventions under investigation include: Oral ferrous sulfate (DIETARY_SUPPLEMENT), Oral placebo tablet (DIETARY_SUPPLEMENT).

Who is sponsoring clinical trial NCT06042699?

This trial is sponsored by Columbia University, which has 958 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06042699 being conducted?

This trial has 1 study location across New York. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.