Last updated: August 23, 2018
Sponsor: Xidian University
Overall Status: Active - Recruiting
Phase
N/A
Condition
Premature Ejaculation
Treatment
N/AClinical Study ID
NCT03583112
81471811
Ages 18-64 Male Accepts Healthy Volunteers
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
right-handed male Chinese volunteers
intravaginal ejaculatory latency time within 1 min
premature ejaculation diagnostic tool score >11 for patients, but <5 for each control.
patients who never received dapoxetine hydrochloride or other SSRI drugs
Exclusion
Exclusion Criteria:
smokers
had medical,neurological or psychiatric disorders
had alcohol, nicotine, or drug abuse
received any treatment at least 2 weeks before the experiment
Study Design
Total Participants: 100
Study Start date:
July 10, 2018
Estimated Completion Date:
December 31, 2018
Connect with a study center
The ART Center, The Northwest Women's and Children's Hospital,
Xi'an, Shaanxi 710003
ChinaActive - Recruiting
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