Effect of Pelvic Floor Stimulation on the Pelvic Floor Function in Cervical Cancer Patients With Type III Hysterectomy

NCT02492542 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 208

Last updated 2018-03-14

No results posted yet for this study

Summary

The purpose of this study is to investigate the effect of electric stimulation on the pelvic floor function in cervical cancer patients with type III hysterectomy.

Conditions

  • Lower Urinary Tract Symptoms

Interventions

DEVICE

PHENIX USB 8.

Electrical stimulation program: frequency: 1/4/Hertz (HZ), pulse width: 270/230/270 μs, time: 30min. Electrode piece: 50\*50mm sticky electrode plate. Position: an electrode piece is placed in the S3, and an electrode piece is placed in the bladder region.Current intensity adjusted according to the patient's tolerance, the maximum current intensity of the pain was not appropriate, generally not more than 100milliampere(mA).Devices PHENIX USB 8.

Sponsors & Collaborators

  • Peking University

    collaborator OTHER
  • Peking University First Hospital

    collaborator OTHER
  • Peking University Third Hospital

    collaborator OTHER
  • Beijing Hospital

    collaborator OTHER_GOV
  • Chinese PLA General Hospital

    collaborator OTHER
  • Peking University Cancer Hospital & Institute

    collaborator OTHER
  • Chinese Academy of Medical Sciences

    collaborator OTHER
  • Beijing Obstetrics and Gynecology Hospital

    collaborator OTHER
  • Beijing Chao Yang Hospital

    collaborator OTHER
  • Wang Jianliu

    lead OTHER

Principal Investigators

  • Wang J liu, Doctor · Peking University People's Hospital Ob and Gy

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
60 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-04-30
Primary Completion
2018-12-31
Completion
2019-12-31

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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 NCT02492542 on ClinicalTrials.gov