ClinicaliQ Trial Snapshot
- PMCF (Post-Market Clinical Follow-up) Study on The Tether™ in UK (United Kingdom) — Recruiting • NCT05830825.
- A study monitoring safety and effectiveness of The Tether™ device in UK patients undergoing surgery for childhood scoliosis.
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Use This Page For
- Quick orientation before opening the registry record.
- Checking recruitment status, phase and sponsor at a glance.
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What This Trial Is Studying
The goal of this observational study is to collect information about The Tether™ device in participants with progressive idiopathic scoliosis, Lenke Type 1 curves. The main purpose is to provide assessment of: * ongoing safety * probable benefits Participants who will receive The Tether™ during spine surgery will have to attend follow-up visits which are part of standard-of-care. Conditions: Scoliosis Idiopathic Interventions: Vertebral Body Tethering (VBT) Lead Sponsor: LDR Médical SAS Planned Enrollment: 100 participants