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Prevalence of Stool Outlet Obstruction After Laparoscopic Sacrocolpopexie

K

Kantonsspital Aarau

Status

Completed

Conditions

Stool Outlet Obstruction

Treatments

Procedure: nerve-sparing laparaoscopic sacrocolpopexy

Study type

Observational

Funder types

Other

Identifiers

NCT03667521
SACRO-GYN-KSA

Details and patient eligibility

About

The aim was to evaluate the prevalence of stool outlet obstruction after laparoscopic sacrocolpopexie at the Kantonsspital Aarau in a prospective cross-sectional study.

Laparoscopic sacrocolpopexy techniques involving the dissection of the presacral space can compromise fibers of the superior hypogastric plexus. This can contribute to postoperative problems such as incomplete voiding, defecatory dysfunction, pain, and sensory problems. In 2010, the Kantonsspital Aarau has implemented a new nerve-sparing laparoscopic sacrocolpopexy technique. This technique has subjectively reduced the prevalence of stool outlet obstructions but this has not been tested systematically yet. The aim of this study is therefore to compare the patients' subjective conditions between these two surgical techniques using the investigator's standard-of-care German pelvic floor questionnaire.

Full description

The (pre-) sacral space is characterized by a complex neuroanatomy and surgical intervention in this part of the body is often associated with the dissection of nerve bundels, a procedure which may finally lead to transient defecatory dysfunction. In a earlier study we could show that ~17.8% of patient with laparoscopic sacrocolpopexie developed postoperative constipation within 3-6 months. In november 2010 the Frauenklinik Aarau introduced a novel, nerve-sparing technique of laparoscopic sacrocolpopexie. In this study we assess the pre-and postoperative differences in defecatory dysfunction between the two procedures trough the analysis of our standard of care pelvic floor questionnaire.

Enrollment

55 patients

Sex

Female

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Women affected by symptomatic vault prolapse, who underwent laparoscopic sacrocolpopexy at the KSA
  • informed consent

Exclusion criteria

  • participation in other studies
  • Sacrocolpopexie done by Da Vinci Roboter
  • Patients who had a conversion to laparotomy perioperatively
  • Patients with a recurrence who had to undergo a second surgery
  • Patients who had a relaps operation

Trial design

55 participants in 2 patient groups

non-nerve-sparing laparaoscopic sacrocolpopexy.
nerve-sparing laparaoscopic sacrocolpopexy.
Treatment:
Procedure: nerve-sparing laparaoscopic sacrocolpopexy

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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