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The company suggests a new concept of treatment for PE: Transient inhibition of striated muscle contraction by a transcutaneous stimulation device. This study aim is to evaluate the safety of delivering increasing electrical stimulation intensities to the subject's perineum, using a TENS technique and equipment, followed by a 72-hour postoperative follow-up.
Age
18 - 60 years
Sex
MALE
Healthy Volunteers
Yes
Rambam Health Care Campus
Haifa, Israel
Start Date
November 2, 2016
Primary Completion Date
June 30, 2017
Completion Date
June 30, 2017
Last Updated
October 8, 2019
20
ACTUAL participants
TENS Stimulator
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