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Randomized controlled trial for the efficacy of electroacupuncture in the treatment of acute urinary incontinence

Randomized controlled trial for the efficacy of electroacupuncture in the treatment of acute urinary incontinence

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900027846
Enrollment
Unknown
Registered
2019-11-30
Start date
2020-01-01
Completion date
Unknown
Last updated
2019-12-10

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

Conditions

urgency urinary incontinence

Interventions

Sponsors

Guizhou university of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. The diagnosis of UUI was made by urologists who met the diagnostic criteria of UUI. 2. The age of the patient was 18 to 75 years. 3. Frequency of urination, urgency of urination, urinary incontinence, although patients know the meaning of urine, but difficult to control voiding. 4. His vital signs are stable and he is conscious enough to be examined and treated. 5. Participants in this study had a duration of at least 3 months. 6. No drug treatment related to the study and no acupuncture treatment within 1 month prior to the study, or participating in other clinical studies within 2 weeks prior to the study. 7. To sign an informed consent form and volunteer for the study.

Exclusion criteria

Exclusion criteria: 1. Other disease performance is frequent micturition, urgent micturition, the patient with incontinence symptom. 2. Patients with a history of botulinum toxin infection of the bladder or pelvic muscles in the past year. 3. There are currently patients with urinary tract infections or vaginal infections. 4. Patients currently undergoing implantable pelvic stimulator therapy. 5. Electrostimulation is currently being applied to patients in the pelvic region, back and leg areas. 6. The use of the drug during treatment may influence outcome decisions and the use of the drug in this study. 7. Currently participating in clinical research related to gynecology, urinary system or kidney Function. 8. Participants with coagulopathy or taking anticoagulants, or patients with severe heart, liver or kidney damage, or during pregnancy or lactation, or patients who are generally in poor condition and unable to cooperate. 9. Participants with a pacemaker, severely afraid of needles, fainting or metal allergy.

Design outcomes

Primary

MeasureTime frame
Urine incontinence questionnaire summary score;Mean number of urgent incontinence within 24 hours;Average number of urgent urination in 24 hours;

Secondary

MeasureTime frame
Average urine output in 24 hours;Urinary incontinence quality of life questionnaire (i-qol) score;The average frequency of urination is 24 hours;Urinary incontinence diagnostic questionnaire score;Acupuncture expectation evaluation;

Countries

China

Contacts

Public ContactMo Qian

Guizhou University of Traditional Chinese Medicine

duoduo425@126.com+86 18286180926

Outcome results

None listed

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