Cervical mucus will be collected from patients undergoing IVF
Diagnostic TestPatients undergoing hormonal stimulation for IVF will be sampled for cervical mucus.
NCT Number: NCT04619524
Analysis of proteins from cervical mucus will be done in patients undergoing infertility treatment (fresh or frozen embryo transfer). Cervical mucus will be analysed for potential new biomarkers of endometrium receptivity. Comparison of the peptide spectrum will be done for the pregnant and not pregnant patients.
Interested in participating?
Request InfoUp to 36 year
Female
Interventional
Not applicable
Brno University Hospital, Brno, South Moravian, Czechia
Successful implantation depends on synchronization between a normal functional embryo at the blastocyst developmental stage and a receptive endometrium. The endometrium is receptive to blastocysts during a spatially and temporally restricted time window called the "window of implantation". Failure of the endometrium to attain receptivity is one cause of infertility, and this is not currently assessed during infertility workup due to a lack of reliable markers for receptivity. Better tests are required to assist the clinician with the decision when to defer a transfer and to freeze all embryos. Proteomics, or the analysis of the proteins in any sample, provides physiologically relevant information, since there are many regulatory steps between the transcriptome and functional proteins. Uterine fluid is a protein-rich histotroph that contains, among other components, secretions from the endometrial glands and cleavage products of both the secreted proteins and the glycocalyx. The aim of this study is to assess the highly sensitive mass spectrometer analysis of the proteins from cervical mucus for the detection of defects in endometrial receptivity and search for new endometrial receptivity biomarkers.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
- Arm A - stimulated cycle:
Exclusion criteria
- Arm A - stimulated cycle:
Inclusion criteria
- Arm B - substituted cycle:
Exclusion criteria
- Arm B - substituted cycle:
Patients undergoing hormonal stimulation for IVF will be sampled for cervical mucus.
Patients undergoing hormonal substitution for transfer of cryopreserved embryos will be sampled for cervical mucus.
Time frame: 48 months
Highly sensitive mass analysis of the proteins from cervical mucus on Thermo Orbitrap Elite instrument for all collected samples.
Time frame: 48 months
Comparison of the protein analysis (qualitative and quantitative) will be done between the pregnant and not pregnant patients. Pregnant patients will be followed-up until child delivery.
Time frame: 48 months
Proteomic endometrial receptivity biomarkers will be detected based on the analysis of measured data in relation to the successful implantation.
Contact information is provided by the study sponsor or research team.
Petr Dzubak, MD.PhD.
CONTACT
Radovan Pilka, Prof.MD.PhD.
CONTACT
The Institute of Molecular and Translational Medicine, Czech Republic
Other
Biomarkers of Endometrial Receptivity: A Prospective Multicenter Study on Proteomic Biomarkers of Endometrial Receptivity in Cervical Mucus ( PRO BIOMER - CM )
Acronym: BIOMER
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT07499817
Embryo Transfer, Genital Diseases
Banī Suwayf, Beni Suweif Governorate, Egypt
View Trial DetailsNCT05364528
Embryo Transfer, Fertility Issues
View Trial DetailsNCT04854707
Female Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications
Barnaul, Russia
View Trial DetailsNCT05969574
Abortion, Habitual, Abortion, Spontaneous
Abu Dhabi, Abu Dhabi Emirate, United Arab Emirates
View Trial Details