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A long term prospective randomized comparative study between TVT and TVT-O in patients of hypermobility stress urinary incontinence

A long term comparative study on efficacy, quality of life and sexual function between TVT and TVT-O in patients of hypermobility stress urinary incontinence: prospective randomized comparative trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-14004371
Enrollment
Unknown
Registered
2014-02-16
Start date
2004-08-18
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

Stress urinary incontinence

Interventions

TVT:Operate the surgical procedure of TVT
TOT:Operate the surgical procedure of TOT

Sponsors

Peking Union Medical College Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
26 Years to 81 Years

Inclusion criteria

Inclusion criteria: Patients with severe to moderate hypermobility stress urinary incontinence.

Exclusion criteria

Exclusion criteria: Intrinsic sphincter deficiency, MUI, concomitant hysterectomy and pelvic reconstruction surgeries, pregnancy, urinary tract infection, a post void residual volume greater than 100 ml, or a past history of neurological disease, urogenital malignancy, fistula or pelvic radiotherapy.

Design outcomes

Primary

MeasureTime frame
PFIQ-7 score;—

Countries

China

Contacts

Public ContactLan Zhu

Peking Union Medical College Hospital

zhu_julie@vip.sina.com+86 13911714696

Outcome results

None listed

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