Eligibility Module

Eligibility Module

The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.

Eligibility Module path is as follows:

Study -> Protocol Section -> Eligibility Module

Eligibility Module


Ignite Creation Date: 2025-12-24 @ 7:32 PM
Ignite Modification Date: 2025-12-24 @ 7:32 PM
NCT ID: NCT05798403
Eligibility Criteria: Inclusion Criteria: * Meet the American Urological Association (AUA) diagnostic criteria for adult overactive bladder disorder (non-neurogenic) and the Chinese Urological Association's Guidelines for the Diagnosis and Treatment of Urological Diseases in China (2014 edition) for OAB. * Female patients aged 18-75 years. * Duration of illness with OAB ≥ 3 months. * 3≤OABSS≤11. * No abnormality in routine urine tests. * Patients had never received acupuncture treatment. * No mental or intellectual abnormalities, able to understand the provisions of the scales and complete the assessment. * Consent to participate in this study and sign a written informed consent. Exclusion Criteria: * Combination of more serious heart, liver, kidney and other serious diseases; Or patients with severe liver or kidney insufficiency. * Patients with pelvic organ prolapse ≥ Ⅱ degree, urinary system surgery history or pelvic floor surgery history. * Patients with other diseases presenting with OAB symptoms. * Those with urinary diseases (such as calculi and tuberculosis of the bladder), malignant tumors, and neurological disorders. * Patients who are pregnant or breastfeeding. * Patients using medication that may affect bladder function one month prior to enrollment or having received behavioural therapy for OAB three months prior to enrolment, etc. * Patients with pacemakers. * Patients with blood diseases, diabetes mellitus or mental diseases. * Infections, ulcers, abscesses, and skin infections at needling sites; metal allergy or extreme needle phobia. * Participation in other clinical medical trial studies over the last month.
Healthy Volunteers: False
Sex: FEMALE
Minimum Age: 18 Years
Maximum Age: 75 Years
Study: NCT05798403
Study Brief:
Protocol Section: NCT05798403