Study Comparing a Cohort of Women Having a Classic Caesarean to a Cohort of Women Having a FAUCS Caesarean (FAUCS)

Ramsay Générale de Santé

Status

Enrolling

Conditions

Cesarean Section; Dehiscence

Extra Peritoneal Caesarean Section

Treatments

Procedure: Caesarean

Study type

Interventional

Funder types

Other

Identifiers

NCT05536869

2019-A01220-57

Details and patient eligibility

About

The main objective of this study is to compare the time taken to obtain "street fitness" status for women after extraperitoneal cesarean section compared to women after a classic cesarean section.

Enrollment

72 estimated patients

Sex

Female

Ages

18 to 42 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Patient scheduled for a caesarean between 38 and 42 weeks pregnant
Patient aged between 18 and 42 years old
Singleton
Caesarean section with a theoretical operating time < 1 hour (without major complications)
Patient affiliated to a social security scheme
Patient having signed the free and informed consent.

Exclusion criteria

BMI > 40
High blood pressure treated intravenously
Pre-existing diabetes in pregnancy
Allergy to analgesics
Prenatal depression
Pathological insertion of the placenta (placenta previa or accreta).
History of major pelvic or abdominal surgery (myomectomy, peritonitis) other than caesarean section or minor surgery.
Addiction (drugs)
Pre-existing psychiatric pathology leading to a risk of impaired judgment or behavior.
Patient participating in another clinical study with a drug or medical device
Protected patient: Adult under guardianship, curatorship or other legal protection, deprived of liberty by judicial or administrative decision
Patient hospitalized without consent.