Study Comparing a Cohort of Women Having a Classic Caesarean to a Cohort of Women Having a FAUCS … (NCT05536869) | Clinical Trial Compass
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Study Comparing a Cohort of Women Having a Classic Caesarean to a Cohort of Women Having a FAUCS Caesarean (FAUCS)
France72 participantsStarted 2021-12-27
Plain-language summary
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.
Who can participate
Age range18 Years – 42 Years
SexFEMALE
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
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.
What they're measuring
1
The postoperative time in hours from which the patient stably fulfills the criteria for "street fitness".