Comparison of Laparoscopic Endometrioma Stripping Versus Ethanol Sclerotherapy( CLESS)

Sponsor
Catholic University of the Sacred Heart (Other)
Overall Status
Recruiting
CT.gov ID
NCT04178876
Collaborator
(none)
64
1
2
44.6
1.4

Study Details

Study Description

Brief Summary

The aim of this study is to compare two different laparoscopic surgical techniques (endometrioma stripping vs ethanol sclerotherapy) in terms of ovarian reserve (AMH levels), recurrence rate and pain relief.

Condition or Disease Intervention/Treatment Phase
  • Procedure: ethanol sclerotherapy
  • Procedure: stripping technique
N/A

Detailed Description

Patients with pelvic pain (VAS score≥4) and ultrasound diagnosis of endometrioma > 4cm candidate to surgical removal of endometrioma will be randomized into 2 group. One Group will undergo laparoscopical stripping technique; the other one will undergo laparoscopic aspiration and sclerotherapy using 95% ethanol.

The women will be introduced with both operative options and they will be informed about the randomization . After an elaborate explanation about the study they will sign an informed consent form. the following data will be collected prior the operation: age, gravity & parity, operative history, general medical history, the cyst size, AMH (Anti Mullerian Hormone), symptoms related to endometriosis (through VAS score), fertility history including any fertility treatment in the past and planned pregnancy after the operation.

The laparoscopy will take place in Fondazione Policlinico Gemelli IRCSS, Roma. in the study group the cyst content will be aspirated and flushed with normal saline. 95% sterile ethanol will be instilled into the cyst through a Nelathon catheter. Ethanol will be left in the cyst for 15 min then aspirated as completely as possible following normal saline flushing. In the control group we will follow the standard treatment which is cystectomy.

The women will be followed at 1 , 3 , 6 and 12 months after the surgery.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
64 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Comparison of Laparoscopic Endometrioma Stripping Versus Ethanol Sclerotherapy: Impact on Ovarian Reserve.
Actual Study Start Date :
Sep 13, 2019
Anticipated Primary Completion Date :
Nov 1, 2022
Anticipated Study Completion Date :
Jun 1, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: Aspiration and Sclerotherapy of endometriomas

Aspiration and Sclerotherapy During Laparoscopy Using 95% Ethanol for the Treatment of Endometriomas

Procedure: ethanol sclerotherapy
Endometrioma laparoscopic aspiration and sclerotherapy using 95% ethanol

Active Comparator: laparoscopic stripping technique

cystectomy of endometriomas during laparoscopy

Procedure: stripping technique
Endometrioma laparoscopic cystectomy

Outcome Measures

Primary Outcome Measures

  1. impact on ovarian reserve, in terms of reduction of serum AMH levels [up to 12 months after the laparoscopy]

    The AMH levels will be evaluated 1 month before the surgery and 1, 6 and 12 months after surgery.

Secondary Outcome Measures

  1. endometrioma recurrence rate for the two surgical techniques [up to 12 months after the laparoscopy]

    Ultrasound examination that demonstrate the presence/lack of ovarian cyst with sonographic features of endometrioma in the ovary where the procedure took place.

  2. pain relief after surgery [up to 12 months after the laparoscopy]

    The severity of pelvic pain , assessed using a visual analogue scale with no-pain classified as 0 and worst imaginable pain as 10.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 35 Years
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Women between 18-35 years old

  • Women with ultrasound diagnosis of ovarian endometrioma ≥4cm (with or without deep infiltrating endometriosis)

  • History of dysmenorrhea and/or chronic pelvic pain

  • candidates for elective laparoscopy due to endometriosis.

Exclusion Criteria:
    • Previous surgery for ovarian endometriosis
  • Evidence of premature ovarian failure (follicle stimulating hormone ≥40 international units/L)

  • Endocrinal disorders that might affect ovarian function (e.g., polycystic ovary syndrome, thyroid dysfunction, hyperprolactinemia)

  • Ultrasound suspicious of ovarian malignant disease according IOTA criteria

  • endometrial cyst < 4 cm. • ethanol sensitivity.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Fondazione Policlinico Universitario Agostino Gemelli IRCCS Roma Italy 00168

Sponsors and Collaborators

  • Catholic University of the Sacred Heart

Investigators

  • Principal Investigator: Giovanni Scambia, MD, Fondazione Policlinico Gemelli, IRCSS Università Cattolica del Sacro Cuore, Roma

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Prof. Giovanni Scambia, Professor, Catholic University of the Sacred Heart
ClinicalTrials.gov Identifier:
NCT04178876
Other Study ID Numbers:
  • 2690
First Posted:
Nov 26, 2019
Last Update Posted:
Dec 4, 2019
Last Verified:
Dec 1, 2019
Individual Participant Data (IPD) Sharing Statement:
Yes
Plan to Share IPD:
Yes
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Prof. Giovanni Scambia, Professor, Catholic University of the Sacred Heart
Additional relevant MeSH terms:

Study Results

No Results Posted as of Dec 4, 2019