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Post-market Clinical Follow-up Study of NEMOST V2 Growing Domino
The NEMOST spinal implant is a growth domino intended for the surgical treatment of progressive scoliosis in children. As part of post-market surveillance, EUROS is conducting a retrospective and prospective study to collect clinical and radiological data on the NEMOST growth domino. Retrospective and prospective multicenter post-market surveillance clinical study. This study is interventional, non-randomized, and uncontrolled. The primary objective of this clinical study is to monitor complications related to the NEMOST growth domino during a 5-year postoperative follow-up in patients treated for progressive scoliosis in children. The secondary objective of this clinical study is to monitor the performance of the NEMOST growth domino during a 5-year postoperative follow-up in patients treated for progressive scoliosis in children. The study will include 140 patients.
Age
5 - 17 years
Sex
ALL
Healthy Volunteers
No
Hopital Lenval Nice
Nice, Provence-Alpes-Côte d'Azur Region, France
CHU Pellegrin
Bordeaux, France
Hospices Civils de Lyon
Lyon, France
Hopital Armand Trousseau
Paris, France
Hopital Necker
Paris, France
Start Date
December 19, 2025
Primary Completion Date
December 19, 2033
Completion Date
December 19, 2033
Last Updated
February 11, 2026
140
ESTIMATED participants
NEMOST V2 growing domino
DEVICE
Lead Sponsor
EUROS
NCT07177430
NCT07249502
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
View ClinicalTrials.gov Terms and ConditionsNCT06789029