RecruitingNot applicableNCT06051123
Effects of Probiotics in Amyotrophic Lateral Sclerosis-Frontotemporal Dementia Spectrum Disorder (ALS-FTDSD) Patients
Studying Amyotrophic lateral sclerosis
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Centre hospitalier de l'Université de Montréal (CHUM)
- Principal Investigator
- Genevieve Matte, MDCM, FRCPCRCHUM
- Intervention
- Probiotic(dietary_supplement)
- Enrollment
- 150 enrolled
- Eligibility
- 18 years · All sexes
- Timeline
- 2024 – 2027
Study locations (1)
- Centre Hospitalier de l'Université de Montréal, Montreal, Quebec, Canada
Collaborators
Lallemand Health Solutions
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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