A multicenter study of efficacy and safety of Japanese-style laparoscopic sacrocolpopexy

A multicenter study of efficacy and safety of Japanese-style laparoscopic sacrocolpopexy - A multicenter study of efficacy and safety of Japanese-style laparoscopic sacrocolpopexy

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

JPRN

Registry ID

JPRN-UMIN000037371

Enrollment

300

Registered

2019-07-16

Start date

2018-10-01

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

None listed

Eligibility

Sex/Gender

Female

Inclusion criteria

Inclusion criteria: Among patients scheduled to receive treatment according to the Japanese-style LSC for pelvic organ prolapse, those who could obtain consent for the survey.

Exclusion criteria

Exclusion criteria: Patients who did not obtain consent for this study, patients who underwent concurrent surgery for co-morbidities.

Design outcomes

Primary

Measure	Time frame
1 Anatomical effectiveness with the POP-Q system. 2 Safety evaluation using Clavien-Dindo classification, Prosthesis / Graft Complication Classification Code. 3 Subjective effectiveness using P-QOL	—

Secondary

Measure	Time frame
1 Effects on lower urinary tract symptoms using IPSS 2 Effects on urinary incontinence using ICIQ-SF 3 Effects on OABSS overactive bladder 4 Effects on defecation function using PFDI 5 Effects on sexual function using PISQ-IR	—

Countries

Japan

Contacts

Public ContactTomoko Kuwata

Daiichi Towakai Hospital Femaleurology, urogynecologycenter

kuwatomo1108@gmail.com072-671-1008

Outcome results