NCT07253194Recruiting
Electroacupuncture on Postoperative Urinary Retention After Radical Surgery for Cervical Cancer
Effect of Electroacupuncture on Postoperative Urinary Retention After Radical Surgery for Cervical Cancer： A Randomized Controlled Trial
Source: ClinicalTrials.gov · Last updated 2 Sept 2026
Brief summary (registry, in English)
This is a prospective, blinded, single-center, randomized controlled trial. Investigators will include 208 patients with postoperative urinary retention (POUR) after radical hysterectomy for cervical cancer who have a clear diagnosis and meet the screening criteria. Participants will be randomly divided into the electroacupuncture（EA）group and the sham EA group according to a 1:1 ratio. Each group consists of 104 patients, and all participants will be required to sign a written informed consent form. The TEAS group will be treated with EA based on conventional treatment, and the shamEA group will be treated with sham EA based on conventional treatment. The main outcomes will be to calculate the proportion of patients who successfully removed the urinary catheter, and the secondary indicators will include the change in post-void residual (PVR) volume of the bladder, assessment of urinary tract infection (UTI), and quality of life assessment according to the EORTC QLQ-C30 scale. Evaluation of participant-reported expectations, blinding, compliance, and safety will also be conducted. All analyses will be conducted in accordance with the intention-to-treat principle.
- Status (registry)
- Recruiting
- Study type
- Interventional
- Enrollment
- 208 (estimated)
- First submitted
- 18 Nov 2025
- Start date
- Jan 2026
- Primary completion date
- Nov 2028
- Lead sponsor
- Lu Chao
- Diseases
- Cervical cancer
- NCT number
- NCT07253194
What you commit to
- Study type: Interventional
- Planned participants: 208
- From Jan 2026 to the primary completion date, Nov 2028
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- ③ Patients who are intolerant to electrical stimulation therapy, such as those with pacemakers installed;
- ⑥ Those who are participating in other acupuncture or drug clinical trials.
Other illness
- ① Obstructive urinary retention, such as urethral stricture or stones induced urinary system diseases;
- ② Merge other serious systemic diseases, and advanced cachexia patients;
- ④ With psychiatric disorder or severe cognitive impairment;
- ⑤ Severe skin damage, infection, and ulceration at the treatment site;
Who the study is looking for
- ① 18 to 70 years old;
- ② Anticipated survival of at least 6 months;
- ③ Met the diagnostic criteria for POUR of cervical cancer, and the duration of POUR is less than 6 months;
- ④ No serious urinary system disease in the past, and no urinary retention before operation;
- ⑤ Karnofsky functional status score (KPS) ≥ 70 points;
- ⑥ Stable vital signs, no serious mental illness, capable of daily living, able to cooperate in completing all treatments and examinations;
- ⑦ Voluntarily participate and sign a written informed consent form.
Age in the registry: 18 years to 70 years · Sex: Female · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Zhejiang Cancer Hospital Coordinator of this site? Confirm its status | Hangzhou | China | Recruiting |
Related publications
This page is information, not medical advice. Discuss any trial with your doctor.