CompletedPHASE2, PHASE3NCT00484510
High Dose Ascorbic Acid Treatment of CMT1A
Studying Charcot-Marie-Tooth disease type 1A
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
- Wayne State University
- Principal Investigator
- Richard A Lewis, MDWayne State University, Dept. of Neurology
- Intervention
- Ascorbic acid (Vitamin C)(drug)
- Enrollment
- 110 enrolled
- Eligibility
- 13-70 years · All sexes
- Timeline
- 2007 – 2012
Study locations (3)
- Johns Hopkins University, Dept of Neurology, Baltimore, Maryland, United States
- Wayne State University, Dept of Neurology, Detroit, Michigan, United States
- University of Rochester Medical Center, Dept of Neurology, Rochester, New York, United States
Collaborators
Muscular Dystrophy Association · Charcot-Marie-Tooth Association
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.
Open NCT00484510 on ClinicalTrials.govOther trials for Charcot-Marie-Tooth disease type 1A
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