Hormonal Monitoring and Progesterone Adjustment in Frozen Embryo Transfer Cycles

Sponsor
Alexandria University (Other)
Overall Status
Completed
CT.gov ID
NCT05189145
Collaborator
(none)
600
1
2
24
25

Study Details

Study Description

Brief Summary

Hormonal monitoring impact on overall pregnancy rate in frozen embryo transfer (FET)cycles and hence progesterone supplement adjustments remain debatable in current literature. This prospective randomized study aims to investigate the effect of monitoring and follow-up of serum progesterone, estradiol & luteinizing hormone (LH) levels and progesterone supplement adjustments on pregnancy outcomes for FET in programmed hormonal replacement therapy cycles in comparison with ultrasound only in control group

Condition or Disease Intervention/Treatment Phase
  • Drug: estradiol valerate
  • Other: Hormonal monitoring progesterone, estradiol, luteinizing hormone
  • Diagnostic Test: transvaginal ultrasound examination
  • Drug: Progesterone 400 Mg Vaginal Suppository
  • Other: Hormonal monitoring progesterone and estradiol
  • Drug: Progesterone
N/A

Detailed Description

Progesterone (P4) is a steroidal hormone that is required for successful embryo implantation and maintenance of the pregnancy in natural cycles, fresh in vitro fertilization cycles, and frozen embryo transfer (FET) cycles. Women undergoing FET in programmed cycle are unable to provide adequate endogenous P4 and require progesterone supplementation to initiate and maintain the secretory endometrium and pregnancy. There has been previous research into luteal phase support in frozen cycles, which has demonstrated that supplementation of progesterone does impact outcome in FET. Despite this evidence for the role of progesterone, there is surprisingly little data on the optimal values for serum P4 during the luteal phase and specifically on the day of embryo transfer in frozen cycles. Following years of a prevalent belief that the higher values of P4 are better, it seems that there may be an optimal window for P4 values during the luteal phase in bovine IVF. Though progesterone levels on the day of transfer have not yet been studied extensively in humans, tailoring the time of transferring a frozen embryo based on serial P4 values rather than cycle day number alone results in higher pregnancy rates. By direct action on the endometrium, a rise of LH might interfere with endometrial receptivity during a FET cycle, in which no pituitary suppression is used. The significance of LH level on the day before addition of progesterone is not yet well defined. The aim of this study is to investigate the effect of monitoring and follow-up of serum progesterone, estradiol & luteinizing hormone levels on day of embryo transfer on pregnancy outcomes for FET in programmed HRT cycles in comparison with ultrasound only in control group and to evaluate the effect of progesterone supplements adjustments depending on serum progesterone levels on day of FET in affecting clinical pregnancy rate.

Study Design

Study Type:
Interventional
Actual Enrollment :
600 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
A Prospective Randomized Study of the Impact of Hormonal Monitoring and Progesterone Supplementation Adjustment on Outcome of Programmed Thawed Embryo Transfer Cycles
Actual Study Start Date :
Oct 1, 2019
Actual Primary Completion Date :
Mar 15, 2021
Actual Study Completion Date :
Oct 1, 2021

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Group I (control)

All patients given 8 mg estradiol valerate orally on daily basis for 13 days beginning with the first day of either a spontaneously or induced menstrual cycle. Patients examined using transvaginal ultrasonography on day 13 of exogenous estrogen supplementation to measure endometrial thickness and to detect signs of escape ovulation. In all Patients progesterone supplements in form of two vaginal prontogest suppositories 400 mg each. Transfer of frozen embryo will be done on day 5 after progesterone supplementation.

Drug: estradiol valerate
8mg orally on daily basis for 13 days beginning with the first day of either a spontaneously or induced menstrual cycle then assess by ultrasound
Other Names:
  • Progenova
  • Diagnostic Test: transvaginal ultrasound examination
    Patients examined using transvaginal ultrasonography on day 13 of exogenous estrogen supplementation to measure endometrial thickness and to detect signs of escape ovulation

    Drug: Progesterone 400 Mg Vaginal Suppository
    Progesterone supplements given in form of daily two vaginal prontogest suppositories400 mg each
    Other Names:
  • prontogest 400 mg vaginal suppository
  • Experimental: group II (experimental)

    All patients given 8 mg estradiol valerate orally on daily basis for 13 days beginning with the first day of either a spontaneously or induced menstrual cycle. Patients examined using transvaginal ultrasonography on day 13 of exogenous estrogen supplementation to measure endometrial thickness and to detect signs of escape ovulation. In all Patients progesterone supplements in form of two vaginal prontogest suppositories 400 mg each. Transfer of frozen embryo will be done on day 5 after progesterone supplementation. progesterone (P4) and estradiol assessed and Progesterone supplement adjustments based on serum level of P4 on day of embryo transfer dividing Group II (Cases) into 3 groups: Group II A: If P4 levels < 5ng/dl, one progesterone supplement in form of 100 mg intramuscular injection daily added Group II B: If P4 levels 5-10ng/dl, dydrogesterone three times daily added Group II C: If P4 levels >10ng, continue on 400 mg prontogest suppositories twice daily

    Drug: estradiol valerate
    8mg orally on daily basis for 13 days beginning with the first day of either a spontaneously or induced menstrual cycle then assess by ultrasound
    Other Names:
  • Progenova
  • Other: Hormonal monitoring progesterone, estradiol, luteinizing hormone
    Serum Progesterone, estrogen & LH measured on day 13 after priming endometrium with 8mg estradiol valerate on a daily basis beginning as early as the first day of menstrual cycle.
    Other Names:
  • P4, E2, LH
  • Diagnostic Test: transvaginal ultrasound examination
    Patients examined using transvaginal ultrasonography on day 13 of exogenous estrogen supplementation to measure endometrial thickness and to detect signs of escape ovulation

    Drug: Progesterone 400 Mg Vaginal Suppository
    Progesterone supplements given in form of daily two vaginal prontogest suppositories400 mg each
    Other Names:
  • prontogest 400 mg vaginal suppository
  • Other: Hormonal monitoring progesterone and estradiol
    Measuring the serum Progesterone & Estradiol in the early morning on the day of embryo transfer an progesterone supplementation adjusted as follows: Group II A: If P4 levels < 5ng/dl, one 100 mg intramuscular injection daily added, Group II B: If P4 levels 5-10ng/dl, dydrogesterone three times daily added. Group II C: If P4 levels >10ng, continued on 400 mg prontogest suppositories twice daily
    Other Names:
  • P4 and E2
  • Drug: Progesterone
    group II A: 100 mg intramuscular injection daily Group II B: If P4 levels 5-10ng/dl dydrogesterone added
    Other Names:
  • prontogest Intramuscular injection, duphaston tab
  • Outcome Measures

    Primary Outcome Measures

    1. live birth rate [assessed 26-40 weeks after embryo transfer]

      the number of live births (defined as at least one live born after 28 weeks of gestation) divided by the total number of patients who performed pregnancy tests

    Secondary Outcome Measures

    1. clinical pregnancy rate [assessed 4 weeks after embryo transfer]

      the number of clinical pregnancies (defined as the presence of a gestational sac with positive heart beat detected by transvaginal ultrasound scan 2 weeks after positive pregnancy test) divided by the number of embryo transfer procedures

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    N/A to 42 Years
    Sexes Eligible for Study:
    Female
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    1. Age of female patient 42 years or less

    2. Normal uterine cavity

    3. All embryos are day 5 or day 6 frozen blastocysts

    Exclusion Criteria:
    1. History of recurrent implantation failure

    2. Previously known major thrombophilia factors

    3. Non-compliance to given protocol

    4. Endometrial thickness < 7mm after 13 days of priming with estradiol valerate

    5. pre-existing metabolic diseases (Diabetes Mellitus & Hypertension).

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Infertility Center Alexandria Egypt

    Sponsors and Collaborators

    • Alexandria University

    Investigators

    • Principal Investigator: Sherif Hebisha, phD, Alexandria University

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    Alexandria University
    ClinicalTrials.gov Identifier:
    NCT05189145
    Other Study ID Numbers:
    • 0201269
    First Posted:
    Jan 12, 2022
    Last Update Posted:
    Jan 31, 2022
    Last Verified:
    Dec 1, 2021
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Alexandria University
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Jan 31, 2022