Clinical Trials Directory

Trials / Completed

CompletedNCT05545774

Neuromuscular Characterisation in Late Adolescent and Adult Cystinosis Patients

Characterization of Neuromuscular Involvement in Late Adolescent and Adult Cystinosis Patients

Status
Completed
Phase
Study type
Observational
Enrollment
20 (actual)
Sponsor
Assistance Publique - Hôpitaux de Paris · Academic / Other
Sex
All
Age
16 Years
Healthy volunteers
Not accepted

Summary

The primary objective of the study is to evaluate the change in motor function of patients with cystinosis. The secondary objectives of the study: * assessment of the respiratory function; * assessment of the muscle function; * assessment of swallowing disorders; * assessment radiologically of the muscular efficiency; * assessment of lean mass / fat mass ratio; * assessment of sleeping disorders; * annual assessment of evolution of above functions. All patients will be examined by experienced neuromuscular specialist (Pr Pascal Laforêt) and pulmonologist specialized in neuromuscular disorders (Pr Hélène Prigent). All evaluations will be performed in Raymond-Poincaré hospital (Teaching hospital of Assistance Publique - Hopitaux de Paris (APHP) and University of Paris-Saclay) neuromuscular center, coordinated by Pr Pascal Laforêt.

Detailed description

This is a monocentric study. The enrollment will be performed as routine care in the department of neurology - neuromuscular center of Raymond Poincaré hospital (APHP). Patients with cystinosis will be consecutively invited to participate in the study until 20 patients are included. This will avoid selection bias if any. For eligible non included patients, a specific non-identifying registry will be set-up with a very restricted number of variables indicative of disease severity at baseline, allowing for a comparison of included and non-included patients. Participating cystinosis patients will be proposed to attend a one-day hospitalization. Evaluations will be performed during stable state upon baseline and during a follow-up visit 12 months later. The study expected duration is 30 months with 18 months for patients' inclusion and 12 month-follow-up.

Conditions

Timeline

Start date
2022-09-22
Primary completion
2025-09-11
Completion
2025-09-11
First posted
2022-09-19
Last updated
2025-11-24

Locations

2 sites across 1 country: France

Source: ClinicalTrials.gov record NCT05545774. Inclusion in this directory is not an endorsement.