Actively Recruiting
Impact of Endometrial Compaction on Reproductive Outcomes After Cryotransfer of Euploid Embryos in a Natural Cycle
Led by Instituto Bernabeu · Updated on 2024-10-03
206
Participants Needed
1
Research Sites
156 weeks
Total Duration
On this page
Sponsors
I
Instituto Bernabeu
Lead Sponsor
U
Universidad Miguel Hernandez de Elche
Collaborating Sponsor
AI-Summary
What this Trial Is About
Multicenter prospective observational cohort study, comparing ongoing pregnancy rates in natural cycles for euploid embryo transfer in patients who present endometrial compaction at the time of the transfer versus those who have a stable or greater endometrial thickness with respect to the estrogenic phase.
CONDITIONS
Official Title
Impact of Endometrial Compaction on Reproductive Outcomes After Cryotransfer of Euploid Embryos in a Natural Cycle
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Aged 18 to 50 years
- Primary or secondary infertility
- Normal uterine cavity
- Undergoing endometrial preparation in a modified natural cycle for single embryo transfer
- Embryo in blastocyst stage from own oocyte or oocyte donation cycles with normal preimplantation genetic testing for aneuploidy results
You will not qualify if you...
- Uterine or endometrial disease such as multiple myomatosis (>3 fibroids >3 cm), adenomyosis, or Asherman syndrome
- Difficulty measuring endometrial thickness due to retroverted or tilted uterus
- History of recurrent implantation failure (3 or more transferred good quality blastocysts) or recurrent early pregnancy loss (2 or more losses before 10 weeks gestation)
- Suboptimal endometrial response with thickness less than 6 mm on day of ovulation triggering
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Instituto Bernabeu
Madrid, Spain, 28001
Actively Recruiting
Research Team
E
Esperanza E de la Torre Pérez, Gynecologist
CONTACT
J
Juan Carlos J Castillo Farfan, Doctor
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
2
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