Infertility, Abortion, Spontaneous, Embryo Implantation, Delayed
Conditions
Brief summary
The main objective of this study is to describe the level of expression of the biological factors involved in the formation of adhesions (Transforming growth factor beta, Activin A, inhibin) at the time of a first diagnostic hysteroscopy among women with synechia, another intracavitary disease or no intracavitary disease.
Detailed description
The secondary obectives are: A. For women who are found to have synechia or another intracavitary pathology at the time of resection: To describe the levels of Transforming growth factor beta, Activin A and Inhibin involved in synechia at the time of resection. B. For women who are found to have synechia or another intracavitary pathology at the time of resection:To describe the levels of Transforming growth factor beta, Activin A and Inhibin involved in synechia at the time of a follow-up hysteroscopy following resection. C. For women who are found to have synechia at the time of resection:To describe the change in levels of Transforming growth factor beta, Activin A and Inhibin involved at the time of a follow-up hysteroscopy following resection whether or not the patient converts back to no synechia. D. For women who are found to have another intracavitary pathology at the time of resection: To describe the change in levels of Transforming growth factor beta, Activin A and Inhibin involved at the time of a follow-up hysteroscopy following resection whether or not the patient converts to synechia. E. To estimate the intra-individual variation in the measured factors (initial biopsy levels versus levels at time of resection). F. To create an intrauterine map of factor levels according to biopy position (riosteal / medium / proximal) for patients with synechia or another intracavitary pathology at the time of resection and then follow-up hysteroscopy. G. To describe the levels of Transforming growth factor beta, Activin A and Inhibin as a function of pregnancy 6 months after resection. H. Create a tissue bank associated with the study.
Interventions
BIOLOGICALHysteroscopy + endometrial biopsy
The day of the first diagnostic hysteroscopy an endometrial biopsy is performed (biopsy A1). These biopsies will be used for the evaluation of TGFbeta, Activin A and inhibin. This intervention is required for the observational needs of this study.
OTHERTelephone call
Patients will be contacted via telephone 6 months after first hysteroscopy. This intervention is required for the observational needs of this study.
BIOLOGICALResection + endometrial biopsy
If patients are found to have synechia or another intracavitary pathology, resection is scheduled 1-2 months later. A second endometrial biopsy is performed at this time. This intervention is required for the observational needs of this study.
BIOLOGICALFollow-up hysteroscopy + endometrial biopsy
For patients having had resection, a follow-up hysteroscopy is performed 1 to 3 months later. An endometrial biopsy will be performed at this time. This intervention is required for the observational needs of this study.
Sponsors
Centre Hospitalier Universitaire de Nīmes
Study design
Observational model
COHORT
Time perspective
PROSPECTIVE
Eligibility
Sex/Gender
FEMALE
Age
18 Years to 44 Years
Healthy volunteers
No
Inclusion criteria
* The patient must be given free and informed consent and must have signed the consent form * The patient must be affiliated with or beneficiary of a health insurance plan * Indication for hysteroscopy associated with one of the following: infertility evaluation, postoperative dysmenorrhea, embryo implantation failure after invitro fertilization, recurrent miscarriages
Exclusion criteria
* The patient is participating in another study * The patient is in an exclusion period determined by a previous study * The patient is under judicial protection, guardianship or curatorship * The patient refuses to sign the consent * It is not possible to correctly inform the patient * The patient is postmenopausal * Indication of hysteroscopy not associated with exploration of infertility or dysmenorrhea * Presence of endometritis objectified via sampling during diagnostic hysteroscopy
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Activin A | Day 0 (day of diagnostic hysteroscopy) |
| Inhibin | Day 0 (day of diagnostic hysteroscopy) |
| Transforming growth factor beta | Day 0 (day of diagnostic hysteroscopy) |
| Diagnosis of synechia or other intracavitary pathology | Day 0 (day of diagnostic hysteroscopy) |
Secondary
| Measure | Time frame |
|---|---|
| Activin A | 1 to 2 months after diagnostic hysteroscopy (day of resection) |
| Pregnancy (yes/no) | 6 months |
| Inhibin | 1 to 2 months after diagnostic hysteroscopy (day of resection) |
| Transforming growth factor beta | 1 to 2 months after diagnostic hysteroscopy (day of resection) |
| Diagnosis of synechia or other intracavitary pathology | 1 to 2 months after diagnostic hysteroscopy (day of resection) |
Countries
France
Outcome results
None listed