← Back to all trials
Recruiting
NCT05830825
PMCF (Post-Market Clinical Follow-up) Study on The Tether™ in UK (United Kingdom)
Conditions: Scoliosis Idiopathic
Sex: All
Ages: 0 Years – 30 Years
Healthy volunteers: No
Enrollment: 100
Sponsor: LDR Médical SAS
Location: Saint George's Hospital London
Summary
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.
Eligibility Criteria
Inclusion Criteria:
* Diagnosis of progressive idiopathic scoliosis;
* Skeletally immature, based on both Risser (\
Source: ClinicalTrials.gov (NCT05830825). StuddyBuddy aggregates publicly available trial information.
