60
Participants
Start Date
July 31, 2012
Primary Completion Date
August 31, 2013
Study Completion Date
February 28, 2014
Cholecalciferol
All patients and physicians were blinded to group assignment and treatment allocation. The first group received oral cholecalciferol of 50,000 IU/week and for 6 months. All subjects were evaluated at baseline and after the end of supplementation for clinical and laboratory parameters.
Placebo
The second group received identical placebo tablets for 6 months. All subjects were evaluated at baseline and after the end of supplementation for clinical and laboratory parameters.
University of Sao Paulo - School of Medicine, São Paulo
ROSA MARIA RODRIGUES PEREIRA
OTHER