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

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

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01581359
Acronym
ENDOFIV
Enrollment
200
Registered
2012-04-20
Start date
2012-03-31
Completion date
2015-05-31
Last updated
2015-10-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Endometriosis, Infertility

Keywords

Endometriosis, GnRH treatment, Infertility, IVF

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.

Interventions

* 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

Sponsors

Instituto de Investigacion Sanitaria La Fe
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 40 Years
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
Clinical pregnancy rate by started cycle2 weeks after biochemical diagnosis of pregnancyNumber of pregnancies with fetal hearth beat on ultrasound exam divided by total number of started cycle

Secondary

MeasureTime frameDescription
Embryo qualityTwo-three days after oocyte recovery and IVF* 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)Day of the Basal ultrasoundTotal 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 / endometriomas37 weeks after cycleNumber of deliveries at 37th to 41st weeks of pregnancy divided by total number of pregnancies
Miscarriage rate22nd week of pregnancyNumber of pregnancy losses divided by total number clinical pregnancies
Number of oocytes retrieved, total and metaphase IIIn the moment of oocyte retrieval
Fertilization rateTwo days after oocyte recovery and IVFNumber of cleavage embryos divided by total number of metaphase II oocytes
Total dose of gonadotropins and days of treatmentDay of the administration of human chorionic gonadotropin (hCG)Total dose of gonadotropins in IU, and total days on treatment
Cancellation rate and causesLast day of gonadotropin treatmentNumber of cancelled cycles divided by total number or started cycles
Ovarian Hyperstimulation Syndrome (OHSS) incidenceOne month after hCGNumber of patients diagnosed of OHSS divided by ended cycles. Classification in mild, moderate and severe
Rate of healthy and live births37th to 41st weeks of pregnancyNumber of healthy and live births divided by total number of started cycle

Countries

Spain

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026