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Study on the therapeutic effect of acupuncture and pelvic floor electrophysiological stimulation on patients with urinary retention after radical resection of cervical cancer

Study on the therapeutic effect of acupuncture and pelvic floor electrophysiological stimulation on patients with urinary retention after radical resection of cervical cancer

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200055297
Enrollment
Unknown
Registered
2022-01-05
Start date
2022-02-01
Completion date
Unknown
Last updated
2023-01-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

urinary retention

Interventions

Sponsors

Obstetrics and Gynecology Hospital Affiliated to Fudan University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. Aged 20-60 years, cervical cancer stage Ib1-IIa2 (2009 FIGO cervical cancer clinical stage), radical hysterectomy, patients with urinary retention after the removal of the urinary catheter 14-60 days after the operation, and the residual urine measurement is greater than 100ml for two consecutive days; 2. The surgical record confirms that the surgical method is radical hysterectomy; 3. The expected survival period is more than 12 months; 4. Agree to participate in this trial and have signed the informed consent.

Exclusion criteria

Exclusion criteria: 1. Patients who have received pelvic radiotherapy in the past; 2. Patients with previous symptoms of urination disorder, urinary incontinence, or abnormal preoperative urodynamic testing; 3. Patients with severe urinary tract infection or vesicovaginal fistula; 4. In the acute phase of other diseases: disturbance of consciousness, body temperature greater than 38°C, unstable vital signs or acute abdomen; 5. Patients with functional impairment of important organs: 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, cardiac function grade 3-4, etc.; 6. Brain disease, abnormal judgment ability; 7. Drug and/or alcohol abuse; 8. Patients with mental illness receiving drug treatment; 9. Participated in other clinical trials within 4 weeks before the start of this study.

Design outcomes

Primary

MeasureTime frame
residual urine;urodynamic measurement;urine routine;

Countries

China

Contacts

Public ContactWang Yun

Obstetrics and Gynecology Hospital Affiliated to Fudan University

yunwang0621@163.com+86 13764418392

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026