Evaluation of Functional Outcomes After Laparoscopic Promontofixation (PFL). (PeSuLife)

C

Caen University Hospital

Status

Unknown

Conditions

Quality of Life
Satisfaction
Pelvic Organ Prolapse
Symptoms

Treatments

Other: Evaluation of laparoscopic promontofixation

Study type

Observational

Funder types

Other

Identifiers

NCT03919123
2018-A02927-48

Details and patient eligibility

About

Prolapse of the pelvic organs is a common pathology in women with a strong impact on the quality of life. Its prevalence tends to increase due to increased life expectancy and obesity. The main treatment is surgical and involves all organ specialists dealing with pelvic-perineal functional disorders: urologists, gynecologists, digestive surgeons. Our team wishes to evaluate, on a cohort of patients operated at the Caen University Hospital, the functional uro-gynecologic, digestive and sexual results of pelvic organ prolapse (POP) repair by Laparoscopic Promontofixation (PFL) through symptoms and quality of life validated questionnaires (QoL). The analysis of the responses to these questionnaires will allow us to evaluate the functional results in the short and medium term (from 6 months to 5 years)

Full description

This is a retrospective cohort study conducted at the Universitary hospital of Caen in three surgical departments (gynecology, urology and digestive surgery). Patients who had a laparoscopic promontofixation will be asked to respond to validated questionnaires of symptoms and quality of life after their surgery (PFDI-20, ICIQ-SF, PFIQ-7) and satisfaction (PGI-I)

Enrollment

200 estimated patients

Sex

Female

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Patients who have had a laparoscopic promotofixation for genital prolapse at the University Hospital of Caen between 2013 and 2018 in the departments of gynecology, urology and digestive surgery.

Patient who received written information and agreed to participate in the study

Exclusion criteria

Minor patient, under guardianship, under trusteeship Patient not understanding French Refusal to participate in the study

Trial contacts and locations

0

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Central trial contact

Estelle Jamard, Doctor

Data sourced from clinicaltrials.gov

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