Condition: Adolescent Idiopathic Scoliosis (AIS) · Neuromuscular Scoliosis · Sponsor: Turku University Hospital
OCTAGON trial is a randomized, double-blinded, parallel-group non-inferiority multicenter (Helsinki and Turku University Hospitals, Finland) clinical trial according to CONSORT criteria. 194 adolescents with idiopathic (major curve \> 45 degrees) or neuromuscular scoliosis (major curve \> 50 degrees) are enrolled for the OCTAGON trial comparing pooled human plasma (Octaplas, 10mL/kg, active management) vs. Plasmalyte (10 mL/kg, placebo) before incision as part of the normal intraoperative fluid therapy. Data is collected at baseline and at each follow-up until a minimum of 2-year follow-up. Outcomes Outcomes for the OCTAGON trial include 1) intraoperative blood loss (in mL, primary outcome) and the need for allogenic red blood cell infusion (percentage of patients). Secondary outcomes include health-related quality of life (Scoliosis Research Society 24 outcome questionnaire), postoperative pain (48-hour opioid consumption), operative time (hours), drain output (mL), hidden blood loss (mL), hospital stay, and complications (skin reactions, TRALI, deep surgical site infection, neurologic deficit). Research questions and hypothesis Does prophylactic use of pooled human plasma decrease intraoperative blood loss in adolescents undergoing instrumented spinal fusion for scoliosis? We hypothesize that pooled human plasma will reduce intraoperative and total blood loss by 25% resulting in lower need for blood transfusion and fewer surgical site infections. Objectives To compare t…
This description comes directly from the study's public registry record.
Ilkka Helenius, MD, orthopaedic surgeon · +358443380034 · ilkka.helenius@helsinki.fi
Tanja Perokorpi, MSc · +358504286559 · tanja.perokorpi@hus.fi
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| Helsinki University Hospital | Helsinki, Finland | Recruiting |
| Turku University Hospital | Turku, Finland | Recruiting |
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Source record: clinicaltrials.gov/study/NCT06934278