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:
2025-12-25 @ 2:46 AM
Ignite Modification Date:
2025-12-25 @ 2:46 AM
NCT ID:
NCT04059133
Eligibility Criteria:
Inclusion Criteria:
1. Women patients within 20\~75 years old;
2. OAB symptoms for ≥ 3 months;
3. Frequency of micturition ≥ 8 times daytime as well as 2 times nighttime, and ≥ 2 episodes of urgency per week;
4. Patients have a ≥ 3 month history of experiencing Stress Urinary Incontinence (SUI) per week (self reported);
5. Patients with OAB symptoms including urgency or/and urgency incontinence, urinary frequency and nocturia in the previous 3 months without medical treatments: antimuscarinic or ß3 agonist therapy;
6. Patients can understand, obey order and finish the questionnaires;
7. Patients would like to sign the informed consent;
8. Signature of informed consent form.
Exclusion Criteria:
1. Urinary tract infection (UTI) at screening and recurrent UTI defined as ≥ 3 UTIs in the previous 12 months;
2. Patients who have other disease: diabetes mellitus, spinal cord injury, stoke history, brain disease and neurogenic disease which can cause OAB;
3. Chronic urologic inflammatory condition (Interstitial cystitis, urethral syndrome, painful bladder syndrome);
4. Bladder stone;
5. History of carcinoma of the urinary tract;
6. Lower urinary tract surgery in the last 6 months;
7. Patients who have operation, wound or infection around perineum;
8. Patients who have catheterization due to poor voiding function of urine;
9. Patients who have severe cardiovascular disease;
10. Patients who have severe coagulopathy or liver failure or renal failure;
11. Patients who have underlying urologic cancer;
12. Subjects with gross hematuria;
13. Significant bladder outflow obstruction;
14. Previous pelvic radiation therapy or previous, current malignant disease of the pelvic organs or having received intravesical injection or electrostimulation in the past 12 months;
15. Drug or nondrug treatments of OAB (in the previous 14 days), Concomitant medications that affect detrusor activity;
16. Subjects with history of kidneys stones;
17. Treatable condition that could cause urinary incontinence or urgency;
18. Neurological impairment or psychiatric disorder preventing appropriate understanding of consent and ability to comply with site personnel instructions;
19. History of drug or alcohol abuse within the last 12 months;
20. Within 1 month before entering the test and receive low-energy in vitro shock wave treatment process using antibiotics or phosphodiesterase inhibitors type 5 (PDE5i);
21. There are chronic pelvic pains caused by the merger of other diseases or injuries;
22. Urinary incontinence need to install the catheter;
23. Severe cardiopulmonary disease or diabetes is obviously poor control;
24. Obvious coagulation dysfunction or liver and kidney dysfunction.
Healthy Volunteers:
False
Sex:
FEMALE
Minimum Age:
20 Years
Maximum Age:
75 Years
Study:
NCT04059133
Study Brief:
Protocol Section:
NCT04059133