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Surgical Treatment of Progressive Scoliosis With "NEMOST" Growing Rod

NCT02266667 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 20

Last updated 2025-09-08

No results posted yet for this study

Summary

The purpose of this study is to evaluate the performance of the device "NEMOST" on maintaining of the correction of the scoliosis with growth preservation and avoiding iterative surgeries.

Objective of this study is to evaluate the performance of the growing device "NEMOST" associated to physiotherapy at 12 months postoperatively in patients treated for progressive scoliosis and to evaluate its safety.

Conditions

  • Progressive Scoliosis

Interventions

DEVICE

2 NEMOST rods : bilateral vertebral-pelvic implantation

Implantation of two NEMOST rods (bilateral vertebral-pelvic implantation)

DEVICE

1 NEMOST rod :unilateral vertebral-pelvic implantation

Implantation of one NEMOST rod (unilateral vertebral-pelvic implantation)

Sponsors & Collaborators

  • Company EUROS

    collaborator UNKNOWN

  • URC-CIC Paris Descartes Necker Cochin

    collaborator OTHER

  • Assistance Publique - Hôpitaux de Paris

    lead OTHER

Principal Investigators

  • Nejib KHOURI, MD, PhD · Hospital Necker Enfants Malades

Study Design

Allocation
NON_RANDOMIZED
Purpose
OTHER
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
5 Years
Max Age
15 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-04-11
Primary Completion
2018-06-21
Completion
2019-05-15

Countries

  • France

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02266667 on ClinicalTrials.gov