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Clinical Trial Summary

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.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03174470
Study type Interventional
Source Virility Medical Ltd.
Contact
Status Completed
Phase N/A
Start date November 2, 2016
Completion date June 30, 2017

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