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Clinical Trial Summary

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).


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03304808
Study type Interventional
Source Instituto Sexológico Murciano
Contact
Status Completed
Phase N/A
Start date October 1, 2017
Completion date December 1, 2017

See also
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