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NCT04003233: UniPOWR

Limited-efficacy Testing of Spring Distraction System (SDS) and Unilateral One-way Rod (MID-C) for Early Onset Scoliosis

Withdrawn NA Last updated 23 March 2020
What this trial tests

NA trial testing SDS in Early-Onset Scoliosis Deformity of Spine (Disorder). Withdrawn.

Timeline
1 July 2019
Primary endpoint
1 July 2022
1 December 2022

Quick facts

Lead sponsorUMC Utrecht
PhaseNA
StatusWithdrawn
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingsingle
Primary purposetreatment
Start date1 July 2019
Primary completion1 July 2022
Estimated completion1 December 2022
Sites2 locations across Netherlands

Drugs / interventions tested

Conditions studied

Sponsor

UMC Utrecht — full company profile →

Who can join

Adults 6 to 12, any sex, with Early-Onset Scoliosis Deformity of Spine (Disorder) or Idiopathic Scoliosis. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The primary aim of this study is to investigate the limited efficacy of these innovative surgical solutions in treatment of Early Onset Scoliosis (EOS) in terms of maintaining reduction while maintaining spinal growth. The secondary aim is to compare both devices for these and other parameters as well as safety.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of SDS

Trials testing the same drug.

Other UMC Utrecht trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT04003233.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing