Comparison of the clinical efficacy of pelvic reconstruction with transvaginal mesh for pelvic organ prolapse repair: hysterectomy or not?

Status

Active, not recruiting

Phases

Phase 4

Study type

Observational

Source

ChiCTR

Registry ID

ChiCTR-ONRC-12002840

Enrollment

Unknown

Registered

2012-12-10

Start date

2012-06-06

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

hysterectomy:transvaginal pelvic reconstruction+hysterectomy

uterine preservation:transvaginal pelvic reconstruction

Eligibility

Sex/Gender

Male

Age

18 Years to 99 Years

Inclusion criteria

Inclusion criteria: All patients who underwent surgery with the synthetic mesh

Exclusion criteria

Exclusion criteria: Unable to give informed consent to participate

Design outcomes

Secondary

Measure	Time frame
the Pelvic Floor Distress Inventory (PFDI-20);The Pelvic Floor Impact Questionnaire (PFIQ-7);Pelvic Organ Prolapse/Urinary Incontinence Sexual;	—

Primary

Measure	Time frame
Anatomical improvement according to POP-Q score;Anatomical no provement according to POP-Q score;Presence/absence of complication;	—

Countries

China

Contacts

Public ContactSong Yanfeng

zlele@126.com+86 13905909403

Outcome results

None listed

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