Total laparoscopic sacrocolpopexy for patients with pelvic organ prolapse

Total laparoscopic sacrocolpopexy for patients with pelvic organ prolapse - Total laparoscopic sacrocolpopexy for patients with pelvic organ prolapse

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

JPRN

Registry ID

JPRN-UMIN000012859

Enrollment

Registered

2014-01-15

Start date

2013-09-02

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 the efficacy and safety of laparoscopic sacrocolpopexy for patients with pelvic organ prolapse.

Eligibility

Sex/Gender

Female

Inclusion criteria

Inclusion criteria: Patients possessing pelvic organ prolapse ( more than stage III of POP-Q stage) are included in this study and their age should be less than 80. They should be without life-threatning complications and hope this surgery. Uteri should be smaller than new-born infant and can be managed by laparoscopy. It should be demanded to obtain written informed consent.

Exclusion criteria

Exclusion criteria: Patients possessing adhesion around the uterus and having difficulties to perform the designed operation. Those who can not understand the meaning and explanation of this surgery. Other patients that are supposed to be inadequate to enroll this study.

Design outcomes

Primary

Measure	Time frame
Improvement of POP-Q staging, amount of hemorrhage during the procedure	—

Secondary

Measure	Time frame
presence of intra- and post-surgical complications, Values of hemoglobin, whtie blood cell count and CRP, Duration and extent of fever,	—

Countries

Japan

Contacts

Public ContactOsamu Hiraike

The University of Tokyo Obstetrics and Gynecology

wada-gyn@h.u-tokyo.ac.jp03-3815-5411

Outcome results

None listed

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