RecruitingNot ApplicableNCT06147843

French-German Cohort Study to Determine Factors Associated With Weight Loss in Amyotrophic Lateral Sclerosis


Sponsor

University Hospital, Limoges

Enrollment

1,000 participants

Start Date

Sep 17, 2024

Study Type

INTERVENTIONAL

Conditions

Summary

Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disease. Studies have shown the importance of weight loss at the time of diagnosis and during the progression of the disease. However, the pathophysiological mechanisms behind weight loss remain unknown. Identifying these mechanisms could make it possible to propose an effective therapeutic strategy against weight loss for ALS patients, which could improve their survival and quality of life. In this context, the investigators are proposing an innovative multidisciplinary project aimed at structuring a large Franco-German cohort to identify the markers associated with weight loss in ALS. Participants will undergo high quality standard care for ALS patients. In addition, participants will be asked to respond different questionnaires and blood samples will be taken for analysis to identify biological markers.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying Blood sample for people with amyotrophic lateral sclerosis. The study is currently recruiting participants at 7 locations.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

OTHERBlood sample

Blood sample will be taken to identify Genomic, metabolomic, metabolic, neurofilaments, and inflammation markers associated to weight loss


Locations(7)

CHU de Lille

Lille, France

Limoges University Hospital

Limoges, France

Hôpital de la Timone

Marseille, France

Hôpital Gui Chauliac

Montpellier, France

CHU de Nice

Nice, France

Hôpital de la Pitié Salpêtrière

Paris, France

CHU de Tours

Tours, France

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NCT06147843


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