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The Efficacy of Transcutaneous Electrical Nerve Stimulation on LUTS: One Prospective Study.

NCT03634722 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 126

Last updated 2018-12-27

No results posted yet for this study

Summary

The study is a prospective study at a single institution. Investigators create strict inclusion and exclusion criteria, selecting 126 patients who undergo the pelvic reconstructive surgery. 63 patients in the intervention group accept 10 times of the transcutaneous electrical nerve stimulation.

Conditions

  • Pelvic Organ Prolapse

Interventions

DEVICE

PHENIX4-8-8 PLUS

transcutaneous electrical nerve stimulation by PHENIX4-8-8 PLUS

Sponsors & Collaborators

  • Peking University People's Hospital

    lead OTHER

Principal Investigators

  • Xiuli Sun · Beijing Key Laboratory of Female Pelvic Floor Disorders

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
DOUBLE
Model
PARALLEL

Eligibility

Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-01-01
Primary Completion
2019-01-07
Completion
2020-12-11

Countries

  • China

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03634722 on ClinicalTrials.gov