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The Effect of Pre-treatment With GnRH Analogues Prior in Vitro Fertilization in Patients With Endometriosis (ENDOFIV)

Primary Purpose

Endometriosis, Infertility

Status
Completed
Phase
Phase 4
Locations
Spain
Study Type
Interventional
Intervention
Triptorelin acetate
Sponsored by
Instituto de Investigacion Sanitaria La Fe
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Endometriosis focused on measuring Endometriosis, GnRH treatment, Infertility, IVF

Eligibility Criteria

18 Years - 40 Years (Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Infertile women with endometriosis diagnosed by surgery in the previous year to their inclusion in the study with signs of residual disease and/or by the existence of ovarian endometrioma in vaginal ecography who are susceptible to IVF treatment.
  • BMI < 28 Kg/m2
  • Age < 40 years old
  • Signed informed consent to perform IVF and participation in this study

Exclusion Criteria:

  • Follicle stimulating hormone (FSH) 2nd-5th cycle day > 12 IU/L
  • Liver disease (sALAT> 80 IU/L)
  • Kidney disease (creatinine > 130 nmol/L)
  • Other relevant disease that contraindicates a pregnancy

Sites / Locations

  • Human Reproduction Unit of the La Fe University and Politechnic Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

GnRHa

Physiological serum

Arm Description

Triptorelin acetate 3,75 mg subcutaneous injection administered on days 1, 28 and 56 after menstrual cycle.

physiological serum subcutaneous injection with same delivery device and same volume that active comparator ) administered on days 1, 28 and 56 after menstrual cycle.

Outcomes

Primary Outcome Measures

Clinical pregnancy rate by started cycle
Number of pregnancies with fetal hearth beat on ultrasound exam divided by total number of started cycle

Secondary Outcome Measures

Number of oocytes retrieved, total and metaphase II
Embryo quality
A Class: high quality; 4 equal cells, <11% fragmentation, display no irregularities (vacuoles and multinucleation) and normal zona pellucida. B Class: good quality; 2 or 5 cells and <26% fragmentation or 4 cells and 12-25% fragmentation, same or similar size (cells even number), display no irregularities and normal zona pellucida. C Class: intermediate quality; no multinucleation , 3 or 6 cells with <36% fragmentation or 2, 4 and 5 cells with 25-35% fragmentation or inequal size blastomeres or absence/low vacuoles cells or anormal zona pellucida.
Number and size of endometrioma(s)
Total number in each ovary, uni or bilateral cysts and maximum diameter (mm) of the biggest endometrioma
Rate of pregnancy to term in patients with endometriosis / endometriomas
Number of deliveries at 37th to 41st weeks of pregnancy divided by total number of pregnancies
Miscarriage rate
Number of pregnancy losses divided by total number clinical pregnancies
Rate of healthy and live births
Number of healthy and live births divided by total number of started cycle
Fertilization rate
Number of cleavage embryos divided by total number of metaphase II oocytes
Total dose of gonadotropins and days of treatment
Total dose of gonadotropins in IU, and total days on treatment
Cancellation rate and causes
Number of cancelled cycles divided by total number or started cycles
Ovarian Hyperstimulation Syndrome (OHSS) incidence
Number of patients diagnosed of OHSS divided by ended cycles. Classification in mild, moderate and severe

Full Information

First Posted
March 20, 2012
Last Updated
October 21, 2015
Sponsor
Instituto de Investigacion Sanitaria La Fe
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1. Study Identification

Unique Protocol Identification Number
NCT01581359
Brief Title
The Effect of Pre-treatment With GnRH Analogues Prior in Vitro Fertilization in Patients With Endometriosis
Acronym
ENDOFIV
Official Title
A Comparative Study, Randomized, Blinded, About the Effect of Pre-treatment With GnRH Analogues Versus Placebo in Infertile Patients With Endometriosis Undergoing in Vitro Fertilization Treatment
Study Type
Interventional

2. Study Status

Record Verification Date
April 2014
Overall Recruitment Status
Completed
Study Start Date
March 2012 (undefined)
Primary Completion Date
March 2015 (Actual)
Study Completion Date
May 2015 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Instituto de Investigacion Sanitaria La Fe

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of this study is to determine whether the administration of an analogue of gonadotropin-releasing hormone (GnRH) during the three months prior to the performing of an IVF may improve the response to ovarian stimulation, implantation rate and clinical pregnancy rate in patients with endometriosis/ endometriomas.
Detailed Description
Endometriosis is defined as the presence of ectopic endometrial tissue which induces a local inflammatory reaction. Usually, this tissue is located at any level in the pelvic region, but extrapelvic locations have been described. It is a chronic disease whose cause is unknown, although a genetic predisposition has been proven. It is estimated that endometriosis affects 7-15% of women of fertile age, and up to 30-40% of women with endometriosis have infertility. Assisted reproduction techniques (ART) are the treatment of many causes of infertility, including endometriosis. The results of assisted reproduction in women with endometriosis appear to be somewhat worse than those obtained from women without endometriosis. Some authors have proven a significant reduction in implantation and pregnancy rates in these patients. The worst pregnancy rate and implantation is believed to be originated in a poor oocyte quality, which can lead to a lower rate of fertilization. This poor oocyte quality produce poorer quality embryos with a reduced capacity to implant, particularly in severe endometriosis. On the other hand, endometrial receptivity does not appear to contribute to the reduction of results of ART in these women. In an attempt to improve ART outcomes in women with endometriosis, different strategies have been proposed prior to the cycle realization, with different results. Surgical resection of endometriomas (endometriosis cysts) before the cycle of IVF/ICSI may adversely affect the results. On the other hand, careful laparoscopic cystectomy appears not to affect the ovarian response to stimulation. In addition to surgical approaches, have been tried different medical treatments to improve the results of IVF / intracytoplasmatic sperm injection (ICSI) in women with endometriosis. It has been suggested that treatment with Danazol prior to IVF may improve results. Similarly, prolonged treatment with GnRH analogues few months before IVF could improve the implantation and pregnancy rates. Unfortunately, many of these studies were not randomized and / or controlled so that the true value of therapy with GnRH analogues before IVF in women with endometriosis still needs to be valued. A recent meta-analysis showed that a 3-6 month treatment with GnRH analogues before IVF increased 4 times the odds of clinical pregnancy in women with endometriosis. Nevertheless, these results were concluded from 165 patients and 78 pregnancies, included in 3 clinical trials, which was not specifically to patients with endometriomas. The lack of studies with proper design, suggests that there is insufficient evidence at present to establish firm recommendations in this regard. This study will contribute to increasing scientific evidence to recommend or not pretreatment with GnRH agonists before IVF en patients with endometriosis.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Endometriosis, Infertility
Keywords
Endometriosis, GnRH treatment, Infertility, IVF

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
200 (Actual)

8. Arms, Groups, and Interventions

Arm Title
GnRHa
Arm Type
Active Comparator
Arm Description
Triptorelin acetate 3,75 mg subcutaneous injection administered on days 1, 28 and 56 after menstrual cycle.
Arm Title
Physiological serum
Arm Type
Placebo Comparator
Arm Description
physiological serum subcutaneous injection with same delivery device and same volume that active comparator ) administered on days 1, 28 and 56 after menstrual cycle.
Intervention Type
Drug
Intervention Name(s)
Triptorelin acetate
Other Intervention Name(s)
Gonapeptyl Depot 3,75
Intervention Description
Triptorelin acetate Dosing regimen: 1 subcutaneous injection of 3,75 mg/28 days, total of 3 doses Placebo Dosing regimen: subcutaneous injection of the same volume of physiological serum/28 days, total of 3 doses
Primary Outcome Measure Information:
Title
Clinical pregnancy rate by started cycle
Description
Number of pregnancies with fetal hearth beat on ultrasound exam divided by total number of started cycle
Time Frame
2 weeks after biochemical diagnosis of pregnancy
Secondary Outcome Measure Information:
Title
Number of oocytes retrieved, total and metaphase II
Time Frame
In the moment of oocyte retrieval
Title
Embryo quality
Description
A Class: high quality; 4 equal cells, <11% fragmentation, display no irregularities (vacuoles and multinucleation) and normal zona pellucida. B Class: good quality; 2 or 5 cells and <26% fragmentation or 4 cells and 12-25% fragmentation, same or similar size (cells even number), display no irregularities and normal zona pellucida. C Class: intermediate quality; no multinucleation , 3 or 6 cells with <36% fragmentation or 2, 4 and 5 cells with 25-35% fragmentation or inequal size blastomeres or absence/low vacuoles cells or anormal zona pellucida.
Time Frame
Two-three days after oocyte recovery and IVF
Title
Number and size of endometrioma(s)
Description
Total number in each ovary, uni or bilateral cysts and maximum diameter (mm) of the biggest endometrioma
Time Frame
Day of the Basal ultrasound
Title
Rate of pregnancy to term in patients with endometriosis / endometriomas
Description
Number of deliveries at 37th to 41st weeks of pregnancy divided by total number of pregnancies
Time Frame
37 weeks after cycle
Title
Miscarriage rate
Description
Number of pregnancy losses divided by total number clinical pregnancies
Time Frame
22nd week of pregnancy
Title
Rate of healthy and live births
Description
Number of healthy and live births divided by total number of started cycle
Time Frame
37th to 41st weeks of pregnancy
Title
Fertilization rate
Description
Number of cleavage embryos divided by total number of metaphase II oocytes
Time Frame
Two days after oocyte recovery and IVF
Title
Total dose of gonadotropins and days of treatment
Description
Total dose of gonadotropins in IU, and total days on treatment
Time Frame
Day of the administration of human chorionic gonadotropin (hCG)
Title
Cancellation rate and causes
Description
Number of cancelled cycles divided by total number or started cycles
Time Frame
Last day of gonadotropin treatment
Title
Ovarian Hyperstimulation Syndrome (OHSS) incidence
Description
Number of patients diagnosed of OHSS divided by ended cycles. Classification in mild, moderate and severe
Time Frame
One month after hCG

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
40 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Infertile women with endometriosis diagnosed by surgery in the previous year to their inclusion in the study with signs of residual disease and/or by the existence of ovarian endometrioma in vaginal ecography who are susceptible to IVF treatment. BMI < 28 Kg/m2 Age < 40 years old Signed informed consent to perform IVF and participation in this study Exclusion Criteria: Follicle stimulating hormone (FSH) 2nd-5th cycle day > 12 IU/L Liver disease (sALAT> 80 IU/L) Kidney disease (creatinine > 130 nmol/L) Other relevant disease that contraindicates a pregnancy
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
ANA Mª MONZÓ, MD, PhD
Organizational Affiliation
La Fe University Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Human Reproduction Unit of the La Fe University and Politechnic Hospital
City
Valencia
ZIP/Postal Code
46026
Country
Spain

12. IPD Sharing Statement

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The Effect of Pre-treatment With GnRH Analogues Prior in Vitro Fertilization in Patients With Endometriosis

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