Actively Recruiting

Age: 2Years - 10Years
All Genders
NCT01840930

Cohort of Children With Severe Cerebral Palsy

Led by Hospices Civils de Lyon · Updated on 2020-01-18

385

Participants Needed

1

Research Sites

1108 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

" Cohort CP " is a multicentre cohort study, initiated by the Hospices Civils de Lyon in September 2009. Population targeted are children with bilateral cerebral palsy, level GMFCS IV or V, aged from 2 to 10 years at inclusion. They are followed-up during 10 years, at the rhythm of 1 visit per year. At each visit are collected clinical, orthopaedic, radiological and environmental data. The primary objective is to establish the incidence of orthopaedic complications (scoliosis and hip joint) depending on patients' age. Secondary objectives are to describe the sequences over time of these complications and the related pain, to explore the impact of nutrition, surgery, asymmetric postures and environmental factors, and to describe the medical and rehabilitative follow-up of these patients. 385 patients are expected by the end of 2020. We expect of this long-term follow-up to gain tools that permit to improve patient's care and patient's quality of life, by putting in place preventing actions and adapted treatments related to their own pathologies.

CONDITIONS

Official Title

Cohort of Children With Severe Cerebral Palsy

Who Can Participate

Age: 2Years - 10Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Children aged from 2 to 10 years at inclusion
  • Children with bilateral cerebral palsy
  • Grade IV or V of the GMFCS
  • Affiliated with the French healthcare system
  • Oral consent of the parents obtained
Not Eligible

You will not qualify if you...

  • Progressive pathology

AI-Screening

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Trial Site Locations

Total: 1 location

1

Hospices Civils de Lyon - Hôpital Femme Mère Enfant

Bron, France, 69677

Actively Recruiting

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Research Team

I

Isabelle POIROT, PhD

CONTACT

V

Valérie LAUDY

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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