Pitié-Salpêtrière Hospital
Paris, 75013, France
NCT Number: NCT00925847
The purpose of the study is to determine whether lithium is safe and effective in the treatment of ALS
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Notify Me18 year and older
All sexes
Interventional
Phase 2
Paris, 75013, France
Daily doses of lithium, have been found to delay progression of amyotrophic lateral sclerosis (ALS) in a 15-month study of 44 patients with ALS. At the end of the trial, about 30 percent of the patients that took riluzole had died, while all those receiving riluzole plus lithium had survived. the lithium group had slower progression as measure by a test of breathing (FVC) and strength.
This study will determine whether lithium in combination with riluzole delay progression of patients with amyotrophic lateral sclerosis disease in comparison of an historical cohort of ALS patients treated with riluzole alone.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
lithium LP 400mg daily po (doses were adjusted during the study to maintain targeted blood levels.)
Time frame: 15 months
Time frame: 15 months
Time frame: 15 months
Time frame: 15 months
Looking for future studies?
Notify MeAssistance Publique - Hôpitaux de Paris
Other
Open Multicenter Study of Lithium in Patients With Amyotrophic Lateral Sclerosis LISLA
Acronym: LISLA
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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