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A multicenter study for follow-up of complications for women having pelvic reconstruction surgery with mesh/native tissue (Part II)

A multicenter study for follow-up of complications for women having pelvic reconstruction surgery with mesh/native tissue.

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800016784
Enrollment
Unknown
Registered
2018-06-24
Start date
2018-06-30
Completion date
Unknown
Last updated
2018-06-25

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

Conditions

Female pelvic floor dysfunction

Interventions

Cohorts received different pelvic reconstruction surgeries:different pelvic reconstruction surgeries

Sponsors

Peking Union Medical College Hospital, Chinese Academy of Medicine Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: Patients are inferred to 27 tertiary hospitals with the complaint of de novo complications after pelvic reconstructive surgeries using mesh, tape and native tissue between June 2018 and June 2023. The subjects include patients who accept treatment not only at our participating hospitals but also from other hospital.

Exclusion criteria

Exclusion criteria: If the same patient who developed complications after pelvic floor reconstructive surgeries has been diagnosed and reported in 27 participating hospitals, and again treated for "the same code complication in other 26 hospitals, she will be ruled out.

Design outcomes

Primary

MeasureTime frame
Prolapse staging;The CTS coding of postoperative complication;

Secondary

MeasureTime frame
Severity of stress urinary incontinence;

Countries

China

Contacts

Public ContactLan Zhu

Peking Union Medical College Hospital, Chinese Academy of Medicine Sciences

zhu_julie@vip.sina.com+86 13911714696

Outcome results

None listed

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