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The effect of incipient overactive bladder on female sexual function and the sexual function of the partner and Belly Dance of YUN noninvasive approach in OAB

The effect of incipient overactive bladder on female sexual function and the sexual function of the partner

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-INR-17012189
Enrollment
Unknown
Registered
2017-07-30
Start date
2017-07-30
Completion date
Unknown
Last updated
2017-08-21

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

Conditions

Overactive Bladder

Interventions

A:Belly Dance of YUN qd,8weeks
B:pelvic training qd,8weeks
C:tolterodine 4mg qd

Sponsors

The Fifth People's Hospital of Shanghai, Fudan University, China
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 55 Years

Inclusion criteria

Inclusion criteria: no menopause; Written informed consent has been obtained; Patient is willing and able to complete the 3-days micturition diary correctly; Symptoms of OAB (including urinary frequency, urgency with or without urge incontinence); the mean frequency of micturition=8 times per day, the frequency of nocturia=2 times per day, voiding volume<200ml each time; OABSS between 6 to 11, Urgency Score=2; unaltered sexual patner.

Exclusion criteria

Exclusion criteria: with severe cardiac diseases and arrhythmia; 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; with contraindication of anticholinergic therapy, such as urinary retention, gastric retention, uncontrolled angle-closure glaucoma and allergy to Wenglitong capsules; acute urinary tract infection with symptoms during screening period; 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; pregnancy, lactation or prepared to pregnancyrecently gave birth (i.e., within 6 months preceding the referral), had previous prolapse or incontinence surgery, or not beginning sexual activities (due to ethics problems) were excluded from this studysignificant stress incontinence or mixed stress / urge incontinence where stress is the predominant factor as determined by the investigator;PVR>50ml

Design outcomes

Primary

MeasureTime frame
OABSS;

Secondary

MeasureTime frame
FSFI;Electrical detection value of pelvic floor;spousal sexual function scores ;

Countries

China

Contacts

Public ContactYangyun Wang

The Fifth People's Hospital of Shanghai, Fudan University, China

wangyangyun1986@163.com+86 18621766816

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 14, 2026