Electroacupuncture on Postoperative Urinary Retention After Radical Surgery for Cervical Cancer

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age18-70
SponsorLu Chao

About this trial

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.

Eligibility criteria

Qualifiers

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;

Disqualifiers

① Obstructive urinary retention, such as urethral stricture or stones induced urinary system diseases;

② Merge other serious systemic diseases, and advanced cachexia patients;

③ Patients who are intolerant to electrical stimulation therapy, such as those with pacemakers installed;

④ With psychiatric disorder or severe cognitive impairment;

Trial design

Treatments tested in this trial

  • EA intervention
  • Sham EA intervention

Treatment groups

208 Participants
are divided into 2 treatment groups

Locations

This trial has no locations

Sponsors and collaborators

Lu Chao

Lead sponsor

Zhejiang Cancer Hospital

Sponsor institution