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Prospective, non-randomized, controlled, single-center study, to evaluate the efficacy of applied nominal electrical stimulation parameters given to premature ejaculation (PE) patients in order to prolong the ejaculatory latency time which will eventually increase the quality of their sexual life.
Age
18 - 60 years
Sex
MALE
Healthy Volunteers
No
Rambam Health Care Campus
Haifa, Israel
Start Date
January 1, 2017
Primary Completion Date
December 1, 2017
Completion Date
December 1, 2017
Last Updated
June 6, 2017
30
ESTIMATED participants
Functional TENS stimulation
DEVICE
Non-Functional TENS stimulation
DEVICE
Lead Sponsor
Virility Medical Ltd.
NCT07434271
NCT06570135
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
View ClinicalTrials.gov Terms and ConditionsNCT07236632