Endometrial Preparation in Frozen Embryo Transfer Cycles

Reproductive Behavior Clinical Trial

Official title: Endometrial Preparation With Aromatase Inhibitors Versus Estradiol in Frozen Embryo Transfer Cycles

Status Not yet recruiting

Clinical Trial Summary

Comparison of protocols for frozen embryo transfer (ET): One protocol using Estrogen supplements and the second protocol using Letrozole

Clinical Trial Description

Study design. Randomized control trial will be conducted at the IVF Units at Meir Medical Center.

Participants. Patients undergoing frozen embryo transfer (ET) cycle with single blastocyst transfer.

Outcome measures The primary outcome measure is clinical pregnancy rate defined as intrauterine pregnancy with positive fetal heart beat measured 2-3 weeks after positive β-hCG test. Secondary outcome measures include: pregnancy rate (defined as positive beta-hCG test 12-14 days after embryo transfer), implantation rate and miscarriage rate.

Methods.

Patients who are candidates for vitrified-warmed single blastocyst transfer will be recruited for the study after signing informed consent form. Patients will then be randomized to one of the following groups:

The Letrozole group (study group); Women in the Letrozole arm will be treated with Aromatase inhibitors (Letrozole; 2.5 mg per day) starting on the 3rd day of the cycle for 5 days. US scan, blood work for serum Estradiol (E2) and progesterone (P) will initially be examined 3-5 days after the last Letrozole pill. Additional US scans and serum E2+P will be performed according to the treating physician's decision. When US scan demonstrates trilaminar endometrium ≥8 mm and the dominant follicle will be ≥18mm, Human Chorionic Gonadotropin (hCG) will be administred(recommbinant hCG - Ovitrelle 250 mcg) and 3 days later vaginal Endometrin 100mg*3/d will be started. Single vitrified-warmed blastocyst transfer will be performed after completing 4 days of the progesterone supplements (7 days from hCG administration). Patients will continue with progesterone supplements untill a pregnancy test which will be performed 12 days following the embryo transfer. If the pregnancy test comes out positive another test will be administered 2 days later, and viability US scan will be performed 2 weeks later. Luteal support will be taken untill the 9th week of pregnancy.

The Estrogen-Progesterone group (control group):

Endometrial preparation: Estrogen supplements (Estradiol 6mg/d) will start at the 2nd-3rd day of the cycle. First US scan will be performed after 10 days. If necessary, adjusting the estradiol doses will be performed according to the physician's decision. After achieving trilinear endometrial thickness ≥8mm progesterone supplements (Endometrin 100mg*3/d) will be administrated. Embryo transfer will be performed after completing 5 days of progesterone supplements (at the 6th day after starting the progesterone supplements). Patients will continue with progesterone supplements untill pregnancy test which will be performed 12 days following the embryo transfer. If pregnancy test is positive another test will be performed 2 days later, and viability US scan will be performed 2 weeks later. Luteal support will be taken untill the 9th week of pregnancy.

Sample size estimation In order to obtain a significance of 0.05 and a power of 80%, the investigators require 54 patients per group (total 108). This estimation is based on the live birth rate of 30% at the estrogen-progesterone endometrial preparation group compared to 60% at the letrozole preparation group. However, the investigators plan to recruit 100 patients in each group due to cycles with lost to follow up and ET cancellation.

Statistical Analysis:

The investigators will use the Shapiro Wilks test to evaluate the distribution of the data. Comparisons will be analyzed using Student's T test or Mann-Whitney U test when appropriate. Proportions will be compared with Chi Square test or Fisher exact test. P value of less than 0.05 will be considered significant. Multivariate logistic regression analysis will be used to compare continuous variables, while controlling for multiplicity and confounding factors. ;

Related Conditions & MeSH terms

• Reproductive Behavior

• NCT number: NCT03540979
• Study type: Interventional
• Source: Meir Medical Center
• Status: Not yet recruiting
• Phase: N/A
• Start date: June 2018
• Completion date: December 2019