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Vaginal mesh of two different material used for pelvic floor reconstruction in treatment of severe pelvic organ prolapsed: a prospective randomized controlled trial

Vaginal mesh of two different material used for pelvic floor reconstruction in treatment of severe pelvic organ prolapsed: a prospective randomized controlled trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IOR-16008015
Enrollment
Unknown
Registered
2016-02-27
Start date
2016-02-26
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

Pelvic organ prolapse

Interventions

1:light mesh
2:extralight mesh

Sponsors

Peking Union Medical College Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
50 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. POP - Q stage III degree above; 2. postmenopausal women.

Exclusion criteria

Exclusion criteria: 1. Previous surgery for POP; 2. Presence of neurologic disease; 3. Serious contraindications to surgical procedures.

Design outcomes

Primary

MeasureTime frame
the rate of mesh-related complications;—

Secondary

MeasureTime frame
the objective cure rate;—

Countries

China

Contacts

Public ContactZhu Lan
zhu_julie@sina.com+86 13911714696

Outcome results

None listed

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