Actively Recruiting

Age: 18Years +
All Genders
NCT05294029

Neuro-Orthopaedic Disorders During Aging in Patients With Neuromotor Disability

Led by Institut de Sante Parasport Connecte Synergies · Updated on 2022-12-23

2000

Participants Needed

1

Research Sites

613 weeks

Total Duration

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Sponsors

I

Institut de Sante Parasport Connecte Synergies

Lead Sponsor

A

Assistance Publique - Hôpitaux de Paris

Collaborating Sponsor

AI-Summary

What this Trial Is About

People with neuromotor disability (i.e. following an inborn or acquired spinal cord, cerebral or peripheral neurological lesion) are at risk of worsening their neuro-orthopaedic disorders during aging, including fracture risk. Nevertheless, at the present time, the natural evolution of their neuro-orthopedic disorders and the long-term functional impact of their medical and surgical treatments is unknown. The aim of this study is to describe neuro-orthopedic disorders during aging of patients with neuromotor disability, their functional repercussions, their comorbidities and the therapeutic strategies used.

CONDITIONS

Official Title

Neuro-Orthopaedic Disorders During Aging in Patients With Neuromotor Disability

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients 18 years old or older
  • Treated in the Neuro Orthopaedic Unit of the Physical Medicine and Rehabilitation Department at the university hospital
  • Have a neuromotor disability
  • No opposition to participation from the patient or authorized close relative if the patient cannot consent
  • Affiliated with a social security scheme
Not Eligible

You will not qualify if you...

  • Under court protection

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Department of Physical Medicine and Rehabilitation, Raymond Poincaré Hospital, AP-HP

Garches, France, 92380

Actively Recruiting

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Research Team

F

François Genêt, MD-PhD

CONTACT

V

Vincent T Carpentier, MD-MSc

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

1

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