Clinical Trial Details

Trial ID: L0966
Source ID: NCT00977730
Associated Drug: Protandim
Title: The Effect of the Dietary Supplement Protandim on Non-Alcoholic Steatohepatitis: A Randomized, Double Blind, Placebo-Controlled Study
Acronym: NASH
Status: Not recruiting
Study Results: No Results Available
Results: --
Conditions: Non-Alcoholic Steatohepatitis
Interventions: Dietary Supplement: Protandim;Dietary Supplement: Placebo
Outcome Measures: Change in NAS at study completion in the Protandim group compared to the placebo group.nan
Sponsor/Collaborators: University of Colorado, Denver
Gender: All
Age: 18 Yearsnan
Phases: Not applicable
Enrollment: 70
Study Type: Interventional
Study Designs: Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator, Outcomes Assessor), Primary Purpose: Treatment
Start Date: 14/09/2009
Completion Date: --
Results First Posted: --
Last Update Posted: 19 February 2015
Locations: United States
URL: http://clinicaltrials.gov/show/NCT00977730