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A randomized controlled trial for comparing electroacupuncture and warm acupuncture in the treatment of overactive bladder

A randomized controlled trial for comparing electroacupuncture and warm acupuncture in the treatment of overactive bladder

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800018176
Enrollment
Unknown
Registered
2018-09-04
Start date
2017-11-27
Completion date
Unknown
Last updated
2018-09-10

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

Conditions

symptomatic overactive bladder

Interventions

Sponsors

Second Affiliated Hospital of Guiyang College of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Meet the diagnostic criteria for overactive bladder 2. Aged 18-75 years 3. Urinary frequency(Daily average urination times = 8 time) 4. 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. 5. Participate in the study for at least 3 months 6. Signed informed consent and volunteered to participate in this study Note: Patients who meet the above 6 items can only be included in this study

Exclusion criteria

Exclusion criteria: 1. Frequent urination and urgency caused by other diseases; 2. Patients with a history of botulinum bladder or pelvic muscle treatment in the past year; 3. Patients with urinary tract infections or vaginal infections; 4. Patients currently undergoing implantable pelvic stimulater; 5. Electrostimulation is currently being applied to patients in the pelvic region, back and leg areas; 6. Patients with a history of treatment equipment and related medications in this study in the past 4 weeks; 7. Currently participating in clinical research related to gynecology, urinary system or kidney function; 8. Patients 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. With a pacemaker, severely afraid of needles, fainting or metal allergy.

Design outcomes

Primary

MeasureTime frame
Average 24-hour urgency;Average 24-hour urination;OABSS score;

Secondary

MeasureTime frame
Average 24-hour nocturia;Average 24-hour urinary incontinence;

Countries

China

Contacts

Public ContactMO Qian

Guiyang College of Traditional Chinese Medicine

duoduo425@126.com+86 18286180926

Outcome results

None listed

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