Endometrial Receptivity Clinical Trial
Official title:
Microbiome and Endometrial Receptivity in Obese Infertile Women
Verified date | October 2023 |
Source | Instituto Valenciano de Infertilidad, IVI VALENCIA |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational [Patient Registry] |
The objective of this project is the identification and quantification of the main bacterial communities present in the endometrial microbiota in obese infertile patients, to assess if there is an alteration of their composition dependent on the body mass index, and if such alteration it could influence the reduction of endometrial receptivity, demonstrated in obese women. If obese patients have an altered digestive microbiota and, at the same time, a lower endometrial receptivity, the investigator want to assess whether such reduction in receptivity may depend on an alteration in the endometrial microbiota, which in non-obese infertile patients has been shown to negatively influence the reproductive results
Status | Completed |
Enrollment | 80 |
Est. completion date | December 31, 2022 |
Est. primary completion date | September 16, 2021 |
Accepts healthy volunteers | No |
Gender | Female |
Age group | 18 Years to 44 Years |
Eligibility | Inclusion Criteria: - Infertile patients undergoing artificial cycle with HRT. - Normal uterus confirmed by ultrasound (absence of uterine pathology such as submucosal or intramural myomas> 4 cm that deform cavity, endometrial polyps or Müllerian anomalies, or adnexal as communicating hydrosalpinx). - Negative serological tests for HIV, HBV, HCV, RPR Exclusion Criteria: - Taking prescribed antibiotics or using IUDs or contraceptives 3 months prior to taking the sample. NOTE: Patients who have taken prophylactic antibiotics for ovarian puncture may be included at least 1 month before taking the sample. - Age> 45 years - Uncorrected uterine pathology, uncorrected hydrosalpinx - Recurrent miscarriage (=2 spontaneous abortions) or failure of implantation (transfer of 6 embryos in day 3 or 4 blastocysts in a cycle of IVF or donation of oocytes without gestation) - Existence of serious or uncontrolled bacterial, fungal or viral infections that, in the opinion of the principal investigator, could interfere with the participation of the patient in the study or in the evaluation of the results of the study. - Any disease or medical condition that is unstable or could endanger the patient's safety and compliance in the study. |
Country | Name | City | State |
---|---|---|---|
Spain | Ivi Valencia | Valencia |
Lead Sponsor | Collaborator |
---|---|
Instituto Valenciano de Infertilidad, IVI VALENCIA | Igenomix, IVI Barcelona, IVI Bilbao |
Spain,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Microbiological analysis of endometrial fluid samples through massive sequencing | Identification and quantification of the main bacterial communities present in the endometrial microbiota of obese and normal-weight infertile patients through the analysis of the endometrial fluid. | 14 months | |
Secondary | Microbiological analysis of saliva samples through massive sequencing. | Identification and quantification of the main bacterial communities present in the oral microbiota of obese and normal-weight infertile patients through the analysis of saliva samples. | 14 months | |
Secondary | Microbiological analysis of feces samples through massive sequencing. | Identification and quantification of the main bacterial communities present in the intestinal microbiota of obese and normal-weight infertile patients through the analysis of feces samples. | 14 months | |
Secondary | Analysis of endometrial receptivity using niERA | Analysis of the optimal implantation window through the study of the expression of 238 genes involved in receptivity using endometrial fluid samples. | 13 months |
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