Phase
Condition
Endometriosis
Dysfunctional Uterine Bleeding
Infertility
Treatment
GnRH agonist
Clinical Study ID
Ages 18-36 Female
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Women aged 18 to 36 years (women ≥18 years to <36 years) with endometriosis and / oradenomyosis
Having benefited from In vitro fertilisation /intracytoplasmic micro-injection withfreeze 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
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 3mg
Known hypersensitivity to estradiol
Known hypersensitivity to progesterone
Known hypersensitivity to acetylsalicylic acid or other nonsteroidalanti-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 venousthrombo-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 ofsimilar 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.
Study Design
Study Description
Connect with a study center
Hopital Foch
Suresnes, 92150
FranceSite Not Available
Hopital Foch
Suresnes 2973675, 92150
FranceActive - Recruiting

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