6
Participants
Start Date
May 31, 2008
Primary Completion Date
December 31, 2010
Study Completion Date
December 31, 2010
Carvedilol and Placebo
All enrolled participants were randomized to receive Carvedilol or Placebo in a 2-way crossover design. Each intervention was administered over 8 weeks before switching to the alternative intervention. The study was terminated early, and data were not unblinded so participants cannot be reported separately.
University of Toledo, Health Science Campus, Toledo
Site Rhode Island Hospital, Providence
Collaborators (1)
GlaxoSmithKline
INDUSTRY
University of Toledo Health Science Campus
OTHER