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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
NA trial testing SDS in Early-Onset Scoliosis Deformity of Spine (Disorder). Withdrawn.
1 July 2022
Quick facts
| Lead sponsor | UMC Utrecht |
|---|---|
| Phase | NA |
| Status | Withdrawn |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | single |
| Primary purpose | treatment |
| Start date | 1 July 2019 |
| Primary completion | 1 July 2022 |
| Estimated completion | 1 December 2022 |
| Sites | 2 locations across Netherlands |
Drugs / interventions tested
- SDS
- MID-C
Conditions studied
- Early-Onset Scoliosis Deformity of Spine (Disorder) — all drugs for Early-Onset Scoliosis Deformity of Spine (Disorder) →
- Idiopathic Scoliosis — all drugs for Idiopathic Scoliosis →
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.
Verify or expand the search:
- PubMed search for NCT04003233
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
Other trials of SDS
Trials testing the same drug.
- NCT04021784 — Limited-efficacy Testing of SDS and NEMOST for Early Onset Neuromuscular Scoliosis · NA · completed
Other UMC Utrecht trials
Trials by the same sponsor.
- NCT07512336 — A Randomized Intra-Patient Controlled Trial of MagnetOs™ Putty vs Autograft in Instrumented Posterolateral Spinal Fusion · NA · not yet recruiting
- NCT07485985 — Coronary Sinus Reducer Therapy for Persisting Angina · NA · not yet recruiting
- NCT07449052 — Comprehensive Invasive Physiological Evaluation of Obstructive Coronary Artery Disease · NA · not yet recruiting
- NCT05375708 — Systemic Therapy in Combination with Stereotactic Radiotherapy in Patients with Metastatic Colorectal Cancer Up to 10 Me · Phase 2 · suspended
- NCT06898541 — Coronary Sinus Reducer in Coronary Microvascular Disease · NA · enrolling by invitation
Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT04003233 (US National Library of Medicine, public domain)
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by UMC Utrecht
- Last refreshed: 23 March 2020
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