Clinical trial

The Impact of Estrogen Administration Duration on Live Birth Rates in Hormonally Prepared Frozen Embryo Transfer Cycles: A Prospective Controlled Study

Name
498496942
Description
This prospective controlled study aimed to investigate the effect of the duration of estrogen (E2) administration prior to progesterone (P) initiation on live birth rates (LBR) in frozen embryo transfer (FET) cycles. The study was conducted at a single tertiary-care in vitro fertilization (IVF) center and included 486 patients undergoing high-quality frozen blastocyst transfer in a hormone replacement therapy (HRT) cycle. Patients scheduled for E2 therapy were administered either 5-7, 8-10, or 11-13 days of treatment, depending on their presentation day. After the E2-only phase, if the endometrial thickness was above 7mm, P was initiated (daily 300mg of vaginal micronized P tablets), and FET was performed on the 6th day of P treatment. The primary outcome measure was LBR.
Trial arms
Trial start
2020-01-01
Estimated PCD
2021-12-31
Trial end
2023-05-01
Status
Completed
Treatment
E2
micronized E2 at a daily dose of 4-6mg,
Arms:
11-13 days E2 therapy, 5-7 days E2 therapy, 8-10 days E2 therapy
Size
420
Primary endpoint
live birth rate
2 years
Eligibility criteria
Inclusion Criteria: * Exogenous hormone preparation of the endometrial lining * High embryo quality ((≥2BB) according to Alpha criteria * Embryo transfer at the blastocyst stage Exclusion Criteria: * - Patients whose treatments were canceled for any reason before the embryo transfer procedure * Patients who underwent embryo transfer in the cleavage stage * Presence of low-quality (\<2BB) blastocysts * \>15% loss of viability of the embryo during embryo thawing,
Protocol
{'studyType': 'OBSERVATIONAL', 'patientRegistry': False, 'designInfo': {'observationalModel': 'COHORT', 'timePerspective': 'PROSPECTIVE'}, 'enrollmentInfo': {'count': 420, 'type': 'ACTUAL'}}
Updated at
2023-05-22

1 organization

1 product

1 indication

Organization
Akdeniz University
Product
E2