Therapeutic Effect of Acupuncture and Pelvic Floor Electrophysiological Stimulation on Patients with Urinary Retention after Radical Resection of Cervical Cancer

Not Applicable

• Conditions: urinary retention

• Registration Number: ITMCTR2200005505
• Lead Sponsor: Obstetrics & Gynecology Hospital of Fudan University

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 20 February 2023

Recruitment & Eligibility

• Status: Pending
• Sex: Female
• Target Recruitment: Not specified

Inclusion Criteria

1. Cervical cancer stage Ib1-IIa2 (2009 FIGO cervical cancer clinical staging) patients of 20-60 years old who have urinary retention after the catheter is removed 14-60 days after radical hysterectomy, whose residual urine is more than 100ml measured for two consecutive days.
2. The operation record confirmed that the operation method was radical hysterectomy;
3. Patients whoes expected survival time is more than 12 months;
4. Patients who agree to participate in this trial and have signed an informed consent form.

Exclusion Criteria

1. Patients who have received pelvic radiotherapy in the past;
2. Patients older than 60 years old or younger than 20 years old;
3. Patients who undergo radical hysterectomy which have not been confirmed by surgery and pathology;
4. Patients with previous symptoms such as urinary dysfunction, urinary incontinence, or abnormal preoperative urodynamic tests;
5. Patients with severe urinary tract infection or vesicovaginal fistula;
6. Patients who are in the acute stage of other diseases: impaired consciousness, body temperature greater than 38°C, unstable vital signs or acute abdomen, etc.;
7. Patients who have important organ function impairment: liver enzymes> 2 times the upper limit of normal, creatinine> 2 times the upper limit of normal, blood amylase> 2 times the upper limit of normal, heart function grade 3-4, etc.;
8. Patients who have brain disease or abnormal judgment ability;
9. Patients who have drug and/or alcohol abuse;
10. Patients with mental illness receiving medication;
11. Patients who participated in other clinical trials within 4 weeks before the start of this study.

Study & Design

• Study Type: Interventional study
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
urodynamic measurement;urine routine;residual urine;