A systematic review suggests that endometrial compaction may improve clinical pregnancy rates. This study aims to identify the proteomic profile of patients with endometrial compaction undergoing single euploid embryo transfer during artificial endometrial preparation cycles, aiming to identify molecular markers associated with improved receptivity and implantation outcomes. Proteomics, Artificial Endometrial Preparation, Endometrial compaction, Euploid
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. No more than one previous FET, 2. Single euploid embryo transferred D5-6, 3. Artificial Endometrial Preparation (AEP), 4. Endometrial thickness 8-14 mm
Exclusion criteria
Exclusion criteria: 1. Contraindication for exogenous hormone administration, 2. Uterine anomalies, 3. Intrauterine adhesions, 4. Endometrial polyp, 5. Myoma uteri submucous type or myoma distorted uterine cavity, 6. Hydrosalpinx, 7. Pelvic inflammatory disease or Sexual transmitted disease, 8. Use other medications e.g. Aspirin, Prednisolone, Dexamethasone or Low molecular weight heparin
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Proteomic profile On the day of embryo transfer Mass spectrometry-based proteomic analysis using LC-MS/MS to quantify protein expression levels | — |
Secondary
| Measure | Time frame |
|---|---|
| Clinical pregnancy rate 6 weeks after embryo transfer Positive fetal heartbeat detected by transvaginal ultrasound,Proteomic profile in pregnant EC group On the day of embryo transfer Quantitative proteomic analysis using LC-MS/MS of uterine fluid in women with endometrial compaction who achieved clinical pregnancy | — |
Countries
Thailand
Contacts
Department of Obstetrics and Gynecology, Faculty of Medicine, Chulalongkorn University