Y type mesh of two different material used for laparoscopic sacral colpopexy in treatment of severe pelvic organ prolapsed: a prospective randomized controlled trial

Status

Recruiting

Phases

Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR-IIR-16008013

Enrollment

Unknown

Registered

2016-02-26

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:mesh of partially absorbing material

2:light and soft mesh

Eligibility

Sex/Gender

Female

Age

45 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. POP - Q stage III degree above; 2. postmenopausal women; 3. patients with predominantly middle pelvic prolapse.

Exclusion criteria

Exclusion criteria: 1. mesh operation history; 2. Perineal nerve disorder or severe complications unable to receive surgery.

Design outcomes

Primary

Measure	Time frame
the objective cure rate,;	—

Secondary

Measure	Time frame
the rate of mesh related complications;	—

Countries

China

Contacts

Public ContactZhu Lan

zhu_julie@sina.com+86 13651314354

Outcome results

None listed

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