Study Purpose:
Mitochondrial dysfunction occurs early in the course of ALS, and the mitochondria may be an important site for therapeutic intervention. Creatine stabilizes the mitochondrial transition pore, and is important in mitochondrial ATP production. In a transgenic mouse model of ALS, administration of creatine prolongs survival and preserves motor function and motor neurons.
Study Status:
Not recruiting
Disease:
Amyotrophic Lateral Sclerosis (ALS) , Familial ALS , Sporadic ALS
Study Type:
Interventional
Type of Intervention:
Drug Trial
Intervention Name:
Placebo:
Phase:
N/A
Study Chair(s)/Principal Investigator(s):
Jeremy Shefner (SUNY)
Clinicaltrials.gov ID:
Neals Affiliated?
Yes
Coordinating Center Contact Information
Study Sponsor:
Estimated Enrollment:
104
Estimated Study Start Date:
09 / 01 / 2000
Estimated Study Completion Date:
09 / 30 / 2002
Posting Last Modified Date:
05 / 09 / 2019
Date Study Added to neals.org:
05 / 09 / 2019