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NCT06251596 Clinical Trial

What is the Impact of Frozen Embryo Transfer Protocol, on Endometrial Compaction

IVF Clinical Trial

Official title:
What is the Impact of Frozen Embryo Transfer Protocol, on Endometrial Compaction

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT06251596
Other study ID # 0202-20-HYMC
Secondary ID
Status Completed
Phase
First received
Last updated
Start date January 25, 2021
Est. completion date December 31, 2023

Study information
Verified date February 2023
Source Hillel Yaffe Medical Center
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This study aims to evaluate endometrial thickness on the day of the frozen embryo transfer, compared to endometrial thickness on the last day of assessment of the endometrium before exposure to progesterone in respect to the protocols used for endometrial preparation

Description:

247 FET cycles were included in the study. Records of all patients and their cryopreservation embryos were analyzed. Data collection included baseline parameters of age, BMI (kg/m2), type of infertility, parity, lifestyles, and cause of infertility, as well as treatment parameters, including number of embryos transferred, embryo quality and pregnancy outcomes. To reflect the broad range of patients typically encountered in clinical practice, no inclusion/exclusion criteria were applied regarding baseline characteristics.

Recruitment information / eligibility
Status Completed
Enrollment 247
Est. completion date December 31, 2023
Est. primary completion date December 31, 2023
Accepts healthy volunteers
Gender Female
Age group 20 Years to 44 Years
Eligibility Inclusion Criteria: - Exclusion Criteria: Pregnancy

Study Design

Related Conditions & MeSH terms

Locations
Country Name City State
Israel Hillel Yaffe Medical Center Hadera Heifa Region

Sponsors (1)
Lead Sponsor Collaborator
Hillel Yaffe Medical Center

Country where clinical trial is conducted

Israel, 

Outcome
Type Measure Description Time frame Safety issue
Primary Endometrial compaction in each group. Endometrial compaction in each group. 5 years
Secondary Implantation and pregnancy rates in each group Implantation and pregnancy rates in each group 5 years
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