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Ovarian Function After Use of Various Hemostatic Techniques During Treatment for Endometrioma (Endometrioma)

Primary Purpose

Endometriosis Ovary, Laparoscopy, Ovary; Functional Disturbance

Status
Active
Phase
Not Applicable
Locations
Brazil
Study Type
Interventional
Intervention
Laparoscopic treatment for endometrioma Astus©
AMH Level
Transvaginal ultrasound for antral follicle count
Laparoscopic treatment for endometrioma Vicryl®
Laparoscopic treatment for endometrioma Surgicel®
Sponsored by
Faculdade de Ciências Médicas da Santa Casa de São Paulo
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Endometriosis Ovary focused on measuring endometrioma, laparoscopy, ovarian reserve, anti-mullerian hormone

Eligibility Criteria

18 Years - 43 Years (Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Age > 18
  • Regular menstrual cycle (21 to 35 days).
  • Unilateral ovarian cyst suggestive of endometrioma.
  • Endometrioma and indication of laparoscopic surgery for cyst removal due to pelvic pain, infertility or cyst persistence.

Exclusion Criteria:

  • Previous ovarian surgery.
  • Endocrine dysfunction (diabetes, thyroid disorders, hyperprolactinemia, adrenal disease, polycystic ovary syndrome).
  • Use of hormones in the past 3 months.
  • Suspected ovarian malignant tumor requiring oophorectomy.
  • History of chemotherapy or radiotherapy.
  • Coagulation disorders.
  • Pregnancy.
  • Autoimmune disease.

Sites / Locations

  • Universidade Federal da Paraiba

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Active Comparator

Active Comparator

Active Comparator

Arm Label

Bipolar tweezers Astus Medical©

2-0 Vicryl® Suture

Surgicel®

Arm Description

Laparoscopic treatment for endometrioma Astus© will use Bipolar coagulation (bipolar tweezers, Astus Medical ©, Copyright 2015, Tampa FL, USA) with 30 W power and a Valleylab generator (Medronic ©, Copyright 2017, Medtronic Parkway, Minneapolis, USA); the number of coagulated points will be counted, and the time for coagulation will be measured in seconds. Transvaginal ultrasound for antral follicle count and blood collection will be performed in this group of patients before surgery, 1, 3 and 6 months after the procedure to dose AMH level, FSH level and to count the number of antral follicle.

Laparoscopic treatment for endometrioma Vicryl® will use suturing with simple suture (2-0/Vicryl polyglactin absorbable synthetic suture; Ethicon Inc., New Jersey, USA); the number of sutures will be recorded. Transvaginal ultrasound for antral follicle count and blood collection will be performed in this group of patients before surgery, 1, 3 and 6 months after the procedure to dose AMH level, FSH level and to count the number of antral follicle.

Laparoscopic treatment for endometrioma Surgicel® will use Hemostatic matrix (Surgicel® Original Absorbable Hemostat, Ethicon, USA). Transvaginal ultrasound for antral follicle count and blood collection will be performed in this group of patients before surgery, 1, 3 and 6 months after the procedure to dose AMH level, FSH level and to count the number of antral follicle.

Outcomes

Primary Outcome Measures

AMH
Antimullerian hormone levels
AMH
Antimullerian hormone levels
AMH
Antimullerian hormone levels
AMH
Antimullerian hormone levels

Secondary Outcome Measures

AFC
Ultrasound antral follicle counts
AFC
Ultrasound antral follicle counts
AFC
Ultrasound antral follicle counts
AFC
Ultrasound antral follicle counts

Full Information

First Posted
October 31, 2017
Last Updated
July 21, 2020
Sponsor
Faculdade de Ciências Médicas da Santa Casa de São Paulo
Collaborators
Federal University of Paraíba, Irmandade da Santa Casa de Misericordia de Sao Paulo
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1. Study Identification

Unique Protocol Identification Number
NCT03430609
Brief Title
Ovarian Function After Use of Various Hemostatic Techniques During Treatment for Endometrioma
Acronym
Endometrioma
Official Title
Ovarian Function After Use of Various Hemostatic Techniques During Treatment for Endometrioma: A Randomized Control Trial
Study Type
Interventional

2. Study Status

Record Verification Date
July 2020
Overall Recruitment Status
Active, not recruiting
Study Start Date
April 1, 2018 (Actual)
Primary Completion Date
July 1, 2020 (Actual)
Study Completion Date
August 31, 2020 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Faculdade de Ciências Médicas da Santa Casa de São Paulo
Collaborators
Federal University of Paraíba, Irmandade da Santa Casa de Misericordia de Sao Paulo

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
Yes
Product Manufactured in and Exported from the U.S.
Yes
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Background: Endometriosis is defined by the presence of endometrial tissue outside the uterine cavity due to causes not yet fully elucidated. The disease affects approximately 2% of women of reproductive age and is associated with infertility. Approximately 17% to 44% of women with endometriosis exhibit endometrioma, or ovarian endometriosis. Laparoscopic cystectomy is currently considered the gold standard treatment for this problem, resulting in improvement of symptoms, a lower recurrence rate and a higher pregnancy rate among infertile patients. However, several studies have shown that this treatment is not free from risks because it is associated with reduction of the ovarian reserve due to accidental removal of ovarian cortex during stripping of the capsule or damage caused by the coagulation energy during hemostasis, even when performed by experienced surgeons. There is still controversy in the literature as to the cause of the reduction of the ovarian reserve, as the mere presence of endometrioma reduces ovarian function by itself. The aim of this study is to compare the effects of different hemostatic methods on the ovarian function of women subjected to laparoscopic surgery for ovarian endometrioma. Methods: Open-label randomized clinical trial to be conducted at Lauro Wanderley University Hospital from September 2017 to August 2020. Eighty-four patients will be randomly allocated to three groups according to the hemostatic technique used during laparoscopic surgery for ovarian endometrioma: bipolar coagulation, laparoscopic suture and hemostatic matrix. Ovarian function will be assessed by measuring serum anti-Mullerian hormone and follicle-stimulating hormone levels and by ultrasound antral follicle counts before surgery and 1, 3 and 6 months after surgery. The study was approved by the research ethics committee at the Medical Sciences Center, Federal University of Paraíba CAAE no. 71621717.9.0000.8069. Discussion: The present study intends to assess the ovarian function of patients with endometrioma subjected to laparoscopic surgical treatment, comparing different hemostatic techniques like bipolar coagulation versus suture versus hemostatic matrix with objective assessments of bipolar coagulation to avoid bias. Thus, the investigators expect to contribute data likely to dispel doubts on the subject.
Detailed Description
OBJECTIVES To compare the effects of various hemostatic methods on the ovarian function of patients subjected to laparoscopic surgery for ovarian endometrioma through AMH and ultrasound antral follicle count (AFC). METHODS Study design An open-label randomized clinical trial will be performed to compare the impact of hemostatic techniques like bipolar coagulation versus laparoscopic suture versus hemostatic matrix during laparoscopic surgery for ovarian endometrioma on the ovarian follicular reserve. Study setting The study will be conducted at the endoscopic gynecology unit of Lauro Wanderley University Hospital, Federal University of Paraíba in Brazil. Study and data collection period The study will be performed from September 2017 to August 2020. Data will be collected from October 2017 to April 2020. Study population Patients with ovarian cysts suggestive of endometrioma on ultrasound cared for at the outpatient clinic of the HULW endoscopic gynecology unit during the study period. Sample In compliance with the eligibility criteria, consecutive convenience sampling will be performed among patients with ovarian cysts suggestive of endometrioma on ultrasound subjected to laparoscopic surgery and randomized to receive different hemostatic techniques during surgery: bipolar coagulation, laparoscopic suture or hemostatic matrix. Sample size. The sample size was calculated through resources available on the Laboratory of Epidemiology and Statistics website of the Dante Pazzanese Institute. The calculation was based on data provided by Sönmezer et al. In this article, the investigators detected significant difference in the first month postoperative, with 2.72±1.49 AMH measurement among patients who receive hemostatic matrix versus 1.64±0.93 among patients who receive bipolar coagulation. Then the statistical assume that the 1.49 standard deviation for AMH measurement in the first month was significant and was the number that provide a greater sample size when compared with other values from that article. The difference to be detected is 1.08, which corresponds to the mean difference in AMH in the first month between the patients who receive hemostatic matrix and bipolar coagulation. On those grounds, and to achieve adequate statistical power 80%; p=0.05, each group should consist of 23 participants. Considering possible losses, the sample will be increased by 20%, corresponding to 28 participants per group and a total of 84 women. Following inclusion, the participants will be randomized as described below. The sample will be divided into three groups according to the hemostatic technique used: Bipolar coagulation (bipolar tweezers, Astus Medical ©, Copyright 2015, Tampa FL, USA) with 30 W power and a Valleylab generator Medronic ©, Copyright 2017, Medtronic Parkway, Minneapolis, USA; the number of coagulated points will be counted, and the time for coagulation will be measured in seconds. Laparoscopic suturing with simple suture 2-0/Vicryl polyglactin absorbable synthetic suture; Ethicon Inc., New Jersey, USA; the number of sutures will be recorded. Hemostatic matrix Surgicel® Original Absorbable Hemostat, Ethicon, USA. Procedures for randomization. Randomization to receive the various hemostatic techniques bipolar coagulation, laparoscopic suture or hemostatic matrix during laparoscopic surgery for endometrioma will be performed based on a list of sequential numbers from 1 to 84 total number of participants to be randomized generated by a statistician using Random Allocation Software version 2.0 and the letters A, B and C; the statistician will be blinded as to their meaning. Another individual not participating in the study will receive the list of random numbers prepared by the statistician and will attribute a letter to each technique bipolar coagulation, laparoscopic surgery and hemostatic matrix through the lottery method. Next, this same individual will prepare opaque envelopes numbered from 1 to 84, which will contain the group of allocation. At the time of inclusion, each participant will be assigned a number corresponding to their order of entrance in the study. The envelope with the corresponding number will be opened by a nurse at the surgical theater at the time of hemostasis during surgery. Thus, allocation will remain concealed before surgery. Procedures for assessment of the ovarian reserve. The ovarian reserve will be assessed through measurements of AMH levels and ultrasound antral follicle count. The AMH levels will be quantitatively measured via ELISA, Enzyme-Linked Immunosorbent Assay Diagnostic Systems Laboratories, Webster, TX, with a detection sensitivity of 0.006 ng/mL. The participants' sera will be obtained from blood samples after centrifugation for 10 minutes to separate the cell contents and debris. Each serum sample will be transferred to polypropylene tubes and stored at -70ºC. Venous blood samples will be collected before surgery on the day ultrasound is performed for antral follicle count, approximately 1 month before surgery and 1, 3 and 6 months after surgery. The participants will also be subjected to transvaginal ultrasound for antral follicle count before surgery 1 month before surgery and 1, 3 and 6 months after surgery. This test will be performed during the early proliferative stage days 3 to 6 of the menstrual cycle; the size of the endometrioma and the ovary volume will be recorded, and functional cysts or suspected malignant cysts will be ruled out. For measurement of cysts, the average diameter of the three perpendicular ovary dimensions will be considered. For antral follicle count, the total number of follicles with diameters under 9 mm will be considered. The ovary and cyst volumes will be calculated using the equation 4/3 x π x (d/2)3, where d is the average diameter. All ultrasound tests will be performed by the same operator using the same device. Procedures for laparoscopic surgery. Surgery will be performed by the same surgeon, with the participants under general anesthesia and in a semi-lithotomy position. A 10-mm umbilical puncture will be performed for the camera after insufflation of the pneumoperitoneum; three additional 5-mm punctures will be performed on the right iliac fossa, left iliac fossa and suprapubic area for instruments. The intra-abdominal pressure will be kept at approximately 15 mmHg. Endometriosis will be categorized according to the classification formulated by the American Society for Reproductive Medicine - ASRM. In all of the groups, endometrioma will be removed by means of the traction and countertraction techniques. Adhesiolysis will be performed to separate the ovary from the adjacent structures as needed. In case of cyst rupture, the contents will be aspirated, and the site where the endometrioma contents fell will be exhaustively rinsed. In the group allocated to receive bipolar coagulation, hemostasis will be performed using bipolar tweezers as few times as possible, just to control any considerable bleeding, at 30 W; the number of coagulated points will be recorded, and the duration of the procedure at each bleeding point will measured. These parameters will help elucidate possible flaws in previous studies, in which assessments were subjective, without specification of the duration of the coagulation in each point or the number of coagulated points. In the group allocated to receive hemostasis by means of laparoscopic surgery, bipolar coagulation will not be performed, and the procedure will involve simple intraovarian sutures 1 or 2 knots with 2-0 Vicryl; the number of sutures will be counted. In the group allocated to receive hemostasis by means of hemostatic matrix, bipolar coagulation will not be performed, and the sealant will be applied on the ovarian wound surface. Procedures for data collection Data collection instrument. The data will be recorded on standardized forms containing closed-ended questions pre-encoded for entry into the computer. The information corresponding to categorical variables will be pre-encoded. Continuous variables will be expressed in the corresponding numerical values; only at the time of analysis will some be categorized. The forms will be duly stored in specific folders before and after typing and analysis. This task will be under the responsibility of the investigator, who will complete the forms at various time points. Data collection. The data will be collected by the investigator and a collaborator, who is a student from the Institutional Program of Undergraduate Research Scholarships. The collaborator will apply the checklist to candidates according to the eligibility criteria. Next, the study protocol will be applied, and the forms will be completed to record all necessary information. Once completed, the forms will be rigorously reviewed by the investigator to check the collected information against that in the medical records. The time-points for data collection, adequate form completion and review will comply with those indicated in the schedule. Data analysis. Statistical analysis will be performed by the investigator, her supervisors and a statistician using Excel software and the statistical software SPSS for Windows, version 19.0.0. Originally, SPSS was the acronym for Statistical Package for the Social Sciences, but at the present time, it is a part of the software name IBM SPSS®, without indication of any particular meaning. Numerical variables will be compared by means of one-way analysis of variance ANOVA or the Kruskal-Wallis tests according to the normality or non-normality of the distribution. The chi-square or Fisher's tests will be used for categorical variables. DISCUSSION The reduction of ovarian function among patients with endometrioma is still a subject of study, and its cause requires further elucidation. Some authors consider that the presence of endometrioma itself accounts for the impairment of ovarian function. According to other authors, the factor associated with such impairment is the hemostatic method used following stripping of the endometrioma capsule, as some studies indicate that bipolar coagulation causes greater ovarian damage. However, no study has objectively assessed either the number of points requiring coagulation or the duration of coagulation; furthermore, the energy used is not standardized among studies. The present study intends to assess the ovarian function of patients with endometrioma subjected to laparoscopic surgical treatment, comparing different hemostatic techniques (bipolar coagulation versus suture versus hemostatic matrix) with objective assessments of bipolar coagulation to avoid bias. Thus, the investigators expect to contribute data likely to dispel doubts on the subject.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Endometriosis Ovary, Laparoscopy, Ovary; Functional Disturbance, Hemostasis
Keywords
endometrioma, laparoscopy, ovarian reserve, anti-mullerian hormone

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Open-label randomized clinical trial to be conducted at Lauro Wanderley University Hospital, at Federal University of Paraiba, from September 2017 to August 2020. Eighty-four patients will be randomly allocated to three groups according to the hemostatic technique used during laparoscopic surgery for ovarian endometrioma: bipolar coagulation, laparoscopic suture and hemostatic matrix. Ovarian function will be assessed by measuring serum anti-Mullerian hormone and by ultrasound antral follicle counts before surgery and 1, 3 and 6 months after surgery.
Masking
None (Open Label)
Allocation
Randomized
Enrollment
38 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Bipolar tweezers Astus Medical©
Arm Type
Active Comparator
Arm Description
Laparoscopic treatment for endometrioma Astus© will use Bipolar coagulation (bipolar tweezers, Astus Medical ©, Copyright 2015, Tampa FL, USA) with 30 W power and a Valleylab generator (Medronic ©, Copyright 2017, Medtronic Parkway, Minneapolis, USA); the number of coagulated points will be counted, and the time for coagulation will be measured in seconds. Transvaginal ultrasound for antral follicle count and blood collection will be performed in this group of patients before surgery, 1, 3 and 6 months after the procedure to dose AMH level, FSH level and to count the number of antral follicle.
Arm Title
2-0 Vicryl® Suture
Arm Type
Active Comparator
Arm Description
Laparoscopic treatment for endometrioma Vicryl® will use suturing with simple suture (2-0/Vicryl polyglactin absorbable synthetic suture; Ethicon Inc., New Jersey, USA); the number of sutures will be recorded. Transvaginal ultrasound for antral follicle count and blood collection will be performed in this group of patients before surgery, 1, 3 and 6 months after the procedure to dose AMH level, FSH level and to count the number of antral follicle.
Arm Title
Surgicel®
Arm Type
Active Comparator
Arm Description
Laparoscopic treatment for endometrioma Surgicel® will use Hemostatic matrix (Surgicel® Original Absorbable Hemostat, Ethicon, USA). Transvaginal ultrasound for antral follicle count and blood collection will be performed in this group of patients before surgery, 1, 3 and 6 months after the procedure to dose AMH level, FSH level and to count the number of antral follicle.
Intervention Type
Procedure
Intervention Name(s)
Laparoscopic treatment for endometrioma Astus©
Other Intervention Name(s)
Treatment for ovarian endometrioma with bipolar Astus©
Intervention Description
Laparoscopic surgery will be performed by the same surgeon, according to the routine of the service.In all of the groups, endometrioma will be removed by means of the traction and countertraction techniques. Adhesiolysis will be performed to separate the ovary from the adjacent structures as needed. In case of cyst rupture, the contents will be aspirated, and the site where the endometrioma contents fell will be exhaustively rinsed. In the hemostasis , the investigators will use coagulation with bipolar tweezers Astus Medical© in this group.
Intervention Type
Diagnostic Test
Intervention Name(s)
AMH Level
Other Intervention Name(s)
Antimulerian Hormone
Intervention Description
The AMH levels will be quantitatively measured via ELISA, Enzyme-Linked Immunosorbent Assay (Diagnostic Systems Laboratories, Webster, TX), with a detection sensitivity of 0.006 ng/mL. The participants' sera will be obtained from blood samples after centrifugation for 10 minutes to separate the cell contents and debris. Each serum sample will be transferred to polypropylene tubes and stored at -70ºC. Venous blood samples will be collected before surgery (on the day ultrasound is performed for antral follicle count, approximately 1 month before surgery) and 1, 3 and 6 months after surgery.
Intervention Type
Diagnostic Test
Intervention Name(s)
Transvaginal ultrasound for antral follicle count
Other Intervention Name(s)
AFC
Intervention Description
The participants will be subjected to transvaginal ultrasound for antral follicle count before surgery (1 month before surgery) and 1, 3 and 6 months after surgery. This test will be performed during the early proliferative stage (days 3 to 6 of the menstrual cycle); the size of the endometrioma and the ovary volume will be recorded, and functional cysts or suspected malignant cysts will be ruled out. For measurement of cysts, the average diameter of the three perpendicular ovary dimensions will be considered. For antral follicle count, the total number of follicles with diameters under 9 mm will be considered.
Intervention Type
Procedure
Intervention Name(s)
Laparoscopic treatment for endometrioma Vicryl®
Other Intervention Name(s)
Treatment for ovarian endometrioma using vicryl suture
Intervention Description
Laparoscopic surgery will be performed by the same surgeon, according to the routine of the service.In all of the groups, endometrioma will be removed by means of the traction and countertraction techniques. Adhesiolysis will be performed to separate the ovary from the adjacent structures as needed. In case of cyst rupture, the contents will be aspirated, and the site where the endometrioma contents fell will be exhaustively rinsed. In the hemostasis , the investigators will perform suture with 2-0 Vicryl® in this group.
Intervention Type
Procedure
Intervention Name(s)
Laparoscopic treatment for endometrioma Surgicel®
Other Intervention Name(s)
Treatment for ovarian endometrioma using matrix Surgicel®
Intervention Description
Laparoscopic surgery will be performed by the same surgeon, according to the routine of the service.In all of the groups, endometrioma will be removed by means of the traction and countertraction techniques. Adhesiolysis will be performed to separate the ovary from the adjacent structures as needed. In case of cyst rupture, the contents will be aspirated, and the site where the endometrioma contents fell will be exhaustively rinsed. In this group, for hemostasis , the investigators will use matrix Surgicel®
Primary Outcome Measure Information:
Title
AMH
Description
Antimullerian hormone levels
Time Frame
Before surgery
Title
AMH
Description
Antimullerian hormone levels
Time Frame
1month after the surgery
Title
AMH
Description
Antimullerian hormone levels
Time Frame
3 months after the surgery
Title
AMH
Description
Antimullerian hormone levels
Time Frame
6 months after the surgery
Secondary Outcome Measure Information:
Title
AFC
Description
Ultrasound antral follicle counts
Time Frame
Before surgery
Title
AFC
Description
Ultrasound antral follicle counts
Time Frame
1month after the procedure
Title
AFC
Description
Ultrasound antral follicle counts
Time Frame
3 months after the procedure
Title
AFC
Description
Ultrasound antral follicle counts
Time Frame
6 months after the procedure

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
43 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age > 18 Regular menstrual cycle (21 to 35 days). Unilateral ovarian cyst suggestive of endometrioma. Endometrioma and indication of laparoscopic surgery for cyst removal due to pelvic pain, infertility or cyst persistence. Exclusion Criteria: Previous ovarian surgery. Endocrine dysfunction (diabetes, thyroid disorders, hyperprolactinemia, adrenal disease, polycystic ovary syndrome). Use of hormones in the past 3 months. Suspected ovarian malignant tumor requiring oophorectomy. History of chemotherapy or radiotherapy. Coagulation disorders. Pregnancy. Autoimmune disease.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Raquel Araujo, M.D.
Organizational Affiliation
Faculdade de Ciências Médicas da Santa Casa de São Paulo; Universidade Federal da Paraíba
Official's Role
Principal Investigator
Facility Information:
Facility Name
Universidade Federal da Paraiba
City
Joao Pessoa
State/Province
Paraiba
ZIP/Postal Code
58051900
Country
Brazil

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
34478564
Citation
Araujo RSDC, Maia SB, Baracat CMF, Fernandes CQBA, Ribeiro HSAA, Ribeiro PAAG. Ovarian function following use of various hemostatic techniques during treatment for unilateral endometrioma: A randomized controlled trial. Int J Gynaecol Obstet. 2022 Jun;157(3):549-556. doi: 10.1002/ijgo.13912. Epub 2021 Sep 21.
Results Reference
derived

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Ovarian Function After Use of Various Hemostatic Techniques During Treatment for Endometrioma

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