Clinical Trial

Pediatric Outcomes and Recovery With Peri-Operative Iron Supplement Evaluation

Study acronym: PORPOISE
Recruiting
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Summary
Varus-derotation osteotomy (VDRO) is a surgery to prevent or address hip displacement in children. Many children having this surgery have cerebral palsy or other neuromotor disorders, who have a higher rate of malnutrition, including low iron or anemia. This can affect their surgical outcomes, such as increasing their need for blood transfusions. This project aims to develop a preoperative nutritional program for VDRO patients, to improve their surgical outcomes and decrease their need for transfusions. This may include taking iron supplementation for patient with low iron or anemia. Participants will undergo a nutrition program before their surgery.
Protocol Amendment History 2 amendments
This ClinicalTrials.gov record has been amended 2 times since 2025-07-23; most recent amendment 2026-05-11.
Status change: Not Yet Recruiting → Recruiting 2026-04-28
Trial Details
NCT Number NCT07095244
Lead Sponsor University of British Columbia
Collaborators: BC Children's Hospital Research Institute
Conditions Varus-Derotation Osteotomy Surgery, Iron-deficiency Anemia, Pelvic Osteotomy Surgery, Cerebral Palsy
Enrollment 180 participants
Start Date 2025-09-01
Primary Completion 2027-12-31 (estimated)
Study Completion 2027-12-31 (estimated)
Updated on ClinicalTrials.gov 2026-05-14