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Randomized controlled trial on the efficacy and safety of Wenglitong capsules against overactive bladder

Randomized controlled trial on the efficacy and safety of Wenglitong capsules against overactive bladde

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IPR-14005626
Enrollment
Unknown
Registered
2014-12-07
Start date
2014-01-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

Overactive Bladder

Interventions

A:Wegnlitong Capsules
B:Extended-release Tolterodine
C:Wegnlitong Capsules & Extended-release Tolterodine

Sponsors

Shanghai Ninth People's Hospital, Shanghai Jiao Tong University, School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1) female, age ranging from 18 to 75; 2) diagnosed as OAB at out-patient departments; 3) urinary frequency and urinary urgency, with or without urgency urinary incontinence; 4) urine volume per micturition < 200ml; 5) diagnosed as traditional Chinese medicine syndrome of dampness heat and blood stasis (represent yellow and slimy tongue fur); 6) urine routine test excluded urinary tract infection and represented no sign of urinary tract infection 4 weeks before screening; 7) patients were able to complete micturition diary with good compliance.

Exclusion criteria

Exclusion criteria: 1) with severe cardiac diseases and arrhythmia; 2) with severe hepatic and renal diseases, in which case aspartate aminotransferase, alanine aminotransferase and creatinine are 1.5 times greater than the upper limit of normal reference range; 3) with contraindication of anticholinergic therapy, such as urinary retention, gastric retention, uncontrolled angle-closure glaucoma and allergy to Wenglitong capsules; 4) acute urinary tract infection with symptoms during screening period; 5) hematuria with unknown cause, cancer, interstitial cystitis, neurogenic bladder, bladder outlet obstruction, urethral catheterization, brain trauma, thyroid diseases, diabetes mellitus and other diseases which researchers recognized as unsuitable to be included in this trial; 6) pregnancy, lactation or prepared to pregnancy.

Design outcomes

Primary

MeasureTime frame
Overactive bladder symptom score;Micturition diary;

Secondary

MeasureTime frame
Type-B ultrasonic checks;

Countries

China

Contacts

Public ContactMujun Lu
lumujun@163.com+86 13020156427

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Mar 12, 2026