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... participants were randomized into two groups.
Results Twenty-nine participants were randomized.
Participants were randomized equally into treatment and placebo groups, and were followed for 3 months.
Participants were randomized to begin the Alive-PD program immediately or after a six-month delay.
Participants were randomized (3:1 ratio) to receive 1 of 5 doses of intracoronary Ad5.hAC6 or placebo.
Participants were randomized to either an intervention or control arm after their baseline standardized measurement visit.
Intervention: Participants were randomized to have the procedure with or without continuous ultrasound guidance.
Participants were randomized to receive vitamin D-fortified cheese, nonfortified cheese, or no cheese.
Participants were randomized into 3 groups (2 interventions and 1 control).
Participants were randomized to vaginal preparation with either povidone-iodine (n = 80) or saline (n = 80).
Interventions: All participants were randomized to receive either 12U/kg of BTX or placebo saline injections.
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