MedPath

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

Phase 1
Conditions
urgency urinary incontinence
Registration Number
ITMCTR1900002794
Lead Sponsor
Guizhou university of Traditional Chinese Medicine
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending
Sex
All
Target Recruitment
Not specified
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

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.

Study & Design

Study Type
Interventional study
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
rine incontinence questionnaire summary score;Average number of urgent urination in 24 hours;Mean number of urgent incontinence within 24 hours;
Secondary Outcome Measures
NameTimeMethod
Acupuncture expectation evaluation;Urinary incontinence diagnostic questionnaire score;Urinary incontinence quality of life questionnaire (i-qol) score;The average frequency of urination is 24 hours;Average urine output in 24 hours;
© Copyright 2025. All Rights Reserved by MedPath