This study will evaluate the pharmacologic effects of exposure to darifenacin and tolterodine on cardiovascular parameters in healthy subjects 50 years of age and older
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
117
Darifenacin tablets 15 mg once daily
Tolterodine extended release (ER) 4 mg once daily
Placebo tablet once daily
Investigative Site
Phoenix, Arizona, United States
Investigative Site
Tempe, Arizona, United States
Mean heart rate per 24 hours following exposure to darifenacin 15 mg o.d. and tolterodine ER 4 mg o.d., at baseline and Day 7
Time frame: 7 days
Effects of darifenacin and tolterodine compared to placebo on mean heart rate per 24 hours, at baseline and Day 7 Effects of darifenacin, tolterodine and placebo on other cardiovascular parameters at baseline and Day 7
Time frame: 7 days
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Investigative Site
Little Rock, Arkansas, United States
Investigative Site
San Diego, California, United States
Investigative Site
Washington D.C., District of Columbia, United States
Investigative Site
Fort Myers, Florida, United States
Investigative Site
Jacksonville, Florida, United States
Investigative Site
Jupiter, Florida, United States
Investigative Site
Miami, Florida, United States
Investigative Site
Orlando, Florida, United States
...and 11 more locations