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Benefit of Hemostatic Sealant in Preservation of Ovarian Reserve (FLOKIP)

Primary Purpose

Benign Ovarian Cyst, Cystectomy

Status
Not yet recruiting
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
Bipolar coagulation
Coagulation by FLOSEAL haemostatic agent
Sponsored by
University Hospital, Montpellier
About
Eligibility
Locations
Arms
Outcomes
Full info

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

18 Years - 45 Years (Adult)FemaleDoes not accept healthy volunteers

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

Arm Type

Active Comparator

Experimental

Arm Label

BIPOLAR FORCEPS

FLOSEAL

Arm Description

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.

Outcomes

Primary Outcome Measures

Serum anti-Mullerian hormone (AMH) level preoperative
A biological assessment with determination of the serum AMH level will be carried out for each patient during the preoperative consultation.
Serum anti-Mullerian hormone (AMH) level at 3 months
A biological assessment with determination of the serum AMH level will be carried out for each patient, 3 months postoperatively.
Serum anti-Mullerian hormone (AMH) level at 6 months
A biological assessment with determination of the serum AMH level will be carried out for each patient, 6 months postoperatively.

Secondary Outcome Measures

Time to achieve hemostasis
The time is measured in minutes from the end of the cystectomy to the end of hemostasis.
Use of additional hemostatsis technique
Another technique can be used to achieve hemostasis: bipolar forceps, suture or second hemostasis agent. The other technique will be specified if it is used
Blood loss
Blood loss will be measured in ml throughout the surgery.
Intraoperative adverse effects
Adverse effects related to the coagulation procedure will be collected.
Revision surgery for bleeding at the operative site
In the event of bleeding at the operative site, revision surgery may be necessary. In this case the information will be collected.

Full Information

First Posted
August 31, 2021
Last Updated
March 10, 2023
Sponsor
University Hospital, Montpellier
Collaborators
Baxter Healthcare Corporation
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1. Study Identification

Unique Protocol Identification Number
NCT05037552
Brief Title
Benefit of Hemostatic Sealant in Preservation of Ovarian Reserve
Acronym
FLOKIP
Official Title
Additional Benefit of Hemostatic Sealant in Preservation of Ovarian Reserve During Laparoscopic Ovarian Cystectomy
Study Type
Interventional

2. Study Status

Record Verification Date
March 2023
Overall Recruitment Status
Not yet recruiting
Study Start Date
September 30, 2023 (Anticipated)
Primary Completion Date
January 30, 2025 (Anticipated)
Study Completion Date
September 30, 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Hospital, Montpellier
Collaborators
Baxter Healthcare Corporation

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Introduction : The most common technique used for ovarian cystectomy is the stripping technique. After stripping the cyst wall, the subsequent bleeding of the ovarian stromal wound is usually controlled by bipolar coagulation or/and by suturing. However, hemostasis achieved with bipolar coagulation could result in damage to the ovarian reserve. To avoid damage to healthy ovarian tissue, hemostasis using various topical hemostatic agents has been introduced to control post- cystectomy ovarian wound bleeding. Among these, FloSeal (Baxter Healthcare Corporation, Deer- field, IL, USA) is a hemostatic sealant composed of a gelatin-based matrix and thrombin solution. Aim: The aim of the study is to evaluate the impact of topical hemostatic sealants and bipolar coagulation during laparoscopic ovarian benign cyst resection on ovarian reserve by comparing the rates of decrease in anti- Müllerian hormone (AMH). Methods: A randomized prospective data collection was made on women aged 18-45 years who planned to have laparoscopic ovarian cystectomy at one of two institutions (n = 80), Montpellier University Hospital and Nimes University Hospital, France. Patients were randomly divided into two groups treated with either a topical hemostatic sealant (Floseal) or bipolar coagulation for hemostasis. Preoperative, 3-month and 6-month postoperative AMH levels were checked and the rates of decrease of AMH were compared.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Benign Ovarian Cyst, Cystectomy
Keywords
Ovarien cyst, Bipolar, Ovarian reserve, Hemostatic agent, Coelioscopy

7. Study Design

Primary Purpose
Health Services Research
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
100 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
BIPOLAR FORCEPS
Arm Type
Active Comparator
Arm Description
The bipolar forceps allow electrocoagulation and are part of the standard laparoscopy box, delivered by the sterilization service to the gynecology operating room.
Arm Title
FLOSEAL
Arm Type
Experimental
Arm Description
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.
Intervention Type
Procedure
Intervention Name(s)
Bipolar coagulation
Intervention Description
Cystectomy will be done via laparoendoscopic surgery After identifying the correct plane of cleavage, the stripping technique will be used. The cyst wall will be gently pulled down from the remaining ovary with two pairs of atraumatic forceps. Once the whole cyst wall will be separated from the ovary cortex, bleeding of the remaining ovarian stromal tissue will be controlled by bipolar coagulation. Then, the remnant tissue will be examined using irrigation and coagulated with minimal bipolar power (20-W current) on any sites that are bleeding.
Intervention Type
Procedure
Intervention Name(s)
Coagulation by FLOSEAL haemostatic agent
Intervention Description
Cystectomy will be done via laparoendoscopic surgery After identifying the correct plane of cleavage, the stripping technique will be used. The cyst wall will be gently pulled down from the remaining ovary with two pairs of atraumatic forceps. Once the whole cyst wall will be separated from the ovary cortex, bleeding of the remaining ovarian stromal tissue will be controlled by either hemostatic sealants (FloSeal). Using a laparoscopic applicator, FloSeal will be applied to the surface of bleeding sites under direct vision and the ovarian cortex was gently pressed for 2 min with small gauze.
Primary Outcome Measure Information:
Title
Serum anti-Mullerian hormone (AMH) level preoperative
Description
A biological assessment with determination of the serum AMH level will be carried out for each patient during the preoperative consultation.
Time Frame
Between 2 and 17 days before cystectomy
Title
Serum anti-Mullerian hormone (AMH) level at 3 months
Description
A biological assessment with determination of the serum AMH level will be carried out for each patient, 3 months postoperatively.
Time Frame
3 months after the cystectomy
Title
Serum anti-Mullerian hormone (AMH) level at 6 months
Description
A biological assessment with determination of the serum AMH level will be carried out for each patient, 6 months postoperatively.
Time Frame
6 months after the cystectomy
Secondary Outcome Measure Information:
Title
Time to achieve hemostasis
Description
The time is measured in minutes from the end of the cystectomy to the end of hemostasis.
Time Frame
From the end of the cystectomy to the end of hemostasis (up to 1 hour)
Title
Use of additional hemostatsis technique
Description
Another technique can be used to achieve hemostasis: bipolar forceps, suture or second hemostasis agent. The other technique will be specified if it is used
Time Frame
From the end of the cystectomy to the end of hemostasis, during surgery
Title
Blood loss
Description
Blood loss will be measured in ml throughout the surgery.
Time Frame
From the start of the surgery to the end of hemostasis
Title
Intraoperative adverse effects
Description
Adverse effects related to the coagulation procedure will be collected.
Time Frame
From the end of the cystectomy to the end of hemostasis
Title
Revision surgery for bleeding at the operative site
Description
In the event of bleeding at the operative site, revision surgery may be necessary. In this case the information will be collected.
Time Frame
From the end of the cystectomy to the end of hemostasis

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
45 Years
Accepts Healthy Volunteers
No
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
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Martha DURAES, MD
Phone
+334 67 33 65 32
Email
m-duraes@chu-montpellier.fr
First Name & Middle Initial & Last Name or Official Title & Degree
Amélie DENOUEL, CRA
Phone
+334 67 33 55 72
Email
a-denouel@chu-montpellier.fr
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Martha DURAES, MD
Organizational Affiliation
Montpellier University Hospital
Official's Role
Study Director
Facility Information:
Facility Name
CHU de Montpellier
City
Montpellier
ZIP/Postal Code
34295
Country
France
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Martha DURAES, MD
Phone
+334.67.33.65.32
Email
m-duraes@chu-montpellier.fr
First Name & Middle Initial & Last Name & Degree
Martha DURAES, MD
First Name & Middle Initial & Last Name & Degree
Gauthier RATHA, MD
First Name & Middle Initial & Last Name & Degree
Lucie REBEL, MD
First Name & Middle Initial & Last Name & Degree
Clara COMPAN, MD
First Name & Middle Initial & Last Name & Degree
Emmanuelle VINTEJOUX, MD
First Name & Middle Initial & Last Name & Degree
Claire VINCNS, MD
Facility Name
CHU de Nîmes
City
Nîmes
ZIP/Postal Code
30029
Country
France
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Renaud DE TAYRAC, MD PhD
Email
renaud.detayrac@chu-nimes.fr
First Name & Middle Initial & Last Name & Degree
Renaud DE TAYRAC, MD PhD
First Name & Middle Initial & Last Name & Degree
Stéphanie HUBERLAND, MD

12. IPD Sharing Statement

Plan to Share IPD
No
Links:
URL
http://www.baxter.ca/sites/g/files/ebysai1431/files/2018-11/Floseal_EN_FR.pdf
Description
FLOSEAL user guide

Learn more about this trial

Benefit of Hemostatic Sealant in Preservation of Ovarian Reserve

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