Benefit of Hemostatic Sealant in Preservation of Ovarian Reserve (FLOKIP)
Benign Ovarian Cyst, Cystectomy

About this trial
This is an interventional health services research trial for Benign Ovarian Cyst focused on measuring Ovarien cyst, Bipolar, Ovarian reserve, Hemostatic agent, Coelioscopy
Eligibility Criteria
Inclusion Criteria:
- Cyst diameter between 3 and 10cm
- Preoperative AMH level >0,5ng/ml
- Understanding and acceptance of the protocol
Exclusion Criteria:
- Post-menopausal status
- Any suspicious finding of malignant ovarian disease
- Change of contraception method leading to AMH variation
- Allergy to bovine products found before inclusion
- Pregnancy
- Patient who has already participated in the protocol
- Person deprived of liberty by judicial or administrative decision
- Person protected by law, under tutorship or curatorship
- Patient participating in another interventional research on the human person in progress
- Refusal of participation after a period of reflection
- Patient not affiliated or beneficiary of a national health insurance system
Sites / Locations
- CHU de Montpellier
- CHU de Nîmes
Arms of the Study
Arm 1
Arm 2
Active Comparator
Experimental
BIPOLAR FORCEPS
FLOSEAL
The bipolar forceps allow electrocoagulation and are part of the standard laparoscopy box, delivered by the sterilization service to the gynecology operating room.
FLOSEAL® is a hemostatic agent based on gelatin of bovine origin added to thrombin of human origin. It is a recommended medical device in surgical procedures as an adjunct to hemostasis when control of bleeding, arterial jet seepage, ligation or any other conventional method proves impractical or ineffective. During this study, it will be used in 1st intention.