Benefit of GnRH Agonist Before Frozen Embryo Transfer in Patients With Endometriosis and/or Adenomyosis

NCT ID: NCT04356664

Last Updated: 2026-01-16

Basic Information

• Recruitment Status: RECRUITING
• Clinical Phase: PHASE2/PHASE3
• Total Enrollment: 180 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2021-03-18
• Study Completion Date: 2026-06-18

Brief Summary

Women suffering from endometriosis and/or adenomyosis may also suffer from infertility. GnRH agonist injection could improve implantation and therefore increase the pregnancy rate in these patients. This study was designed to evaluate effects of the additional of GnRH agonist (single or 2 doses) to the routine oestrogens and progestins use as support before Frozen Embryon Transfer as compared to oestrogens and progestins only.

Detailed Description

Endometriosis reveals the presence of glands or endometrial stroma outside the uterus, responsible for pain and infertility. Adenomyosis illustrates an invagination of endometrial islets within the myometrium, leading to a disturbance of its contractile activity, also potentiated by local hyperestrogenism.

These two pathologies are often associated, and express an alteration of the eutopic endometrium by pro-inflammatory markers responsible for a lower implantation rate.

GnRH agonists are known to decrease these pro-inflammatory markers (cytochrome P450 and Cox 2 aromatase) in the eutopic endometrium of women with endometriosis or adenomyosis.

Patients will received 1 or 2 injection of GnRH delay agonist (Decapeptyl 3mg) approximately 1 month before the frozen embryo transfer.

Conditions

Endometriosis; Adenomyosis; Infertility, Female

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Frozen embryo transfer with Hormonal Replacement Therapy (HRT)

Patient will received usual Hormonal Replacement Therapy for a Frozen embryo transfer composed of estrogens and progestins.

Group Type: NO_INTERVENTION

No interventions assigned to this group

Frozen embryo transfer with HRT and GnRH agonist

Patient will received 1 or 2 injection of GnRH agonist priori to usual Hormonal Replacement Therapy for a Frozen embryo transfer composed of estrogens and progestins.

Group Type: EXPERIMENTAL

GnRH agonist

Intervention Type: DRUG

One or two intramuscular injections of Decapeptyl 3 mg

Interventions

GnRH agonist

One or two intramuscular injections of Decapeptyl 3 mg

Intervention Type: DRUG

Other Intervention Names

Decapeptyl 3 mg

Eligibility Criteria

Inclusion Criteria

• Women aged 18 to 36 years (women ≥18 years to <36 years) with endometriosis and / or adenomyosis
• Having benefited from In vitro fertilisation /intracytoplasmic micro-injection with freeze all and for whom the frozen embryon transfer of a blastocyst is planned
• A normal uterine cavity
• An MRI showing endometriosis and / or adenomyosis during the inclusion visit
• Having signed a consent form
• Being affiliated to a Health Insurance Plan.

Exclusion Criteria

• Patient aged <18 years and ≥ 36 years
• BMI> 35
• History of implantation failures (≥ 2)
• Endometrial alterations: synechiae, polyps, myomas, hyperplasia, hematometra
• known hydrosalpinx uni or bilateral
• MRI showing no endometriosis or adenomyosis
• Hypersensitivity to GnRH, GnRH analogues, or any of the excipients of Decapeptyl 3 mg
• Known hypersensitivity to estradiol
• Known hypersensitivity to progesterone
• Known hypersensitivity to acetylsalicylic acid or other nonsteroidal anti-inflammatory drugs
• Known hypersensitivity to folic acid
• Known hypersensitivity to cefixime or an antibiotic in the cephalosporin group
• Known hypersensitivity to levofloxacin or any other quinolone
• History of tendinopathies related to the administration of fluoroquinolones
• Epilepsy
• Hypersensitivity to contrast agents for MRI
• Known or suspected breast cancer or history of breast cancer
• Known or suspected genital tract cancer or history of genital cancer
• known or suspected estrogen-dependent malignant neoplasms
• Undiagnosed genital haemorrhage
• Untreated endometrial hyperplasia
• History of idiopathic venous thrombo-embolic accident or evolving venous thrombo-embolic event (deep vein thrombosis, pulmonary embolism)
• Recent or evolving arterial thromboembolic stroke (eg angina, myocardial infarction)
• Acute liver disease or history of liver disease, until hepatic tests are normalized
• Severe renal insufficiency
• Severe, uncontrolled heart failure
• Evolutionary gastroduodenal ulcer
• History of asthma caused by the administration of salicylates or substances of similar activity, especially nonsteroidal anti-inflammatory drugs
• GnRH Agonist Decapeptyl administered within 6 months prior to transfer
• To be deprived of liberty or under guardianship
• Pregnancy and breast feeding.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 36 Years
• Eligible Sex: FEMALE
• Accepts Healthy Volunteers: No

Sponsors

Hopital Foch

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Paul Pirtea, Dr

Role: STUDY_DIRECTOR

Hopital Foch

Locations

Hopital Foch

Suresnes, , France

Site Status: RECRUITING

Countries

France

Central Contacts

Elisabeth Hulier-Ammar, Dr

Role: CONTACT

e.hulier-ammar@hopital-foch.com

0033146251175 ext. +33

Facility Contacts

Paul Pirtea

Role: primary

p.pirtea@hopital-foch.com

+331 46 25 35 20

Other Identifiers

2019_0012

Identifier Type: -

Identifier Source: org_study_id