Premature Ejaculation Clinical Trial
Official title:
A Randomized, Controlled Study of the Efficacy of a New Behavioral Treatment for Premature Ejaculation Using a Masturbation Aid Device
The present study included 57 patients ≥18 years who met diagnostic criteria for PE including
intravaginal ejaculatory latency time (IELT) of ≤2 minutes and had a Premature Ejaculation
Diagnostic Tool (PEDT) score ≥11.
Subjects were randomized to an experimental group that used the device with exercise
programme (n=18) a first control group that only used the exercise programme (n=17) and a
wait-list control group (n=22).
As a main outcome measure used stopwatch-measured average IELT, Premature Ejaculation Profile
(PEP), and the Golombok-Rust Inventory of Sexual Satisfaction (GRISS).
n/a
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