Condition: Scoliosis Idiopathic · Sponsor: LDR Médical SAS
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.
This description comes directly from the study's public registry record.
Delphine Lebrasseur-Longuet · +33 626262240 · ClinicalEMEA@highridgemedical.com
Always discuss trial participation with your own doctor first.
| Saint George's Hospital | London, United Kingdom | Recruiting |
| Freeman Hospital | Newcastle upon Tyne, United Kingdom | Recruiting |
| University Southampton Hospital | Southampton, United Kingdom | Recruiting |
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Source record: clinicaltrials.gov/study/NCT05830825