Clinical and urodynamic study in pelvic organ prolapse patients perioperative laparoscopic sacrocolpopexy A prospective study

Clinical and urodynamic study in pelvic organ prolapse patients perioperative laparoscopic sacrocolpopexy: A prospective study - Evaluation of urinary incontinence in perioperative laparoscopic sacrocolpopexy

Status

Recruiting

Phases

Phase 4

Study type

Interventional

Source

JPRN

Registry ID

JPRN-UMIN000043845

Enrollment

100

Registered

2021-05-01

Start date

2021-04-01

Completion date

Unknown

Last updated

2026-06-29

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

Conditions

Pelvic organ prolapse

Interventions

We evaluate perioperative incontinence for pelvic organ prolapse with incontinence by urodynamic study.

Eligibility

Sex/Gender

Female

Inclusion criteria

Inclusion criteria: POP with incontinence patients are included more than POP-Q stage 2 in this study. Informed consent was obtained from all study participants.

Exclusion criteria

Exclusion criteria: Those who underwent a simultaneous anti-incontinence procedure were excluded. Those who prescribe for antimuscarinics and beta 3-adrenoreceptor agonist during perioperative surgery. Those who are supposed to be inadequate to enroll this study.

Design outcomes

Primary

Measure	Time frame
The primary objective of this study was to evaluate the patient-reported urinary incontinence perioperative laparoscopic sacrocolpopexy.	—

Secondary

Measure	Time frame
The secondary objective was to compare urodynamic study parameters perioperative laparoscopic sacrocolpopexy.	—

Countries

Japan

Contacts

Public ContactHirotaka Sato

Hokusuikai Kinen Hospital Department of Urology

hirotakasato911@yahoo.co.jp0293033003

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026