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Letrozole Versus Hormonal Preparation in Frozen Cycles of PCOS Patients.

Primary Purpose

Frozen Embryo Transfer, Polycystic Ovarian Disease, Letrozole

Status
Not yet recruiting
Phase
Phase 4
Locations
Study Type
Interventional
Intervention
Letrozole 2.5mg
Sponsored by
Dubai Fertility Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Frozen Embryo Transfer

Eligibility Criteria

20 Years - 40 Years (Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Women with PCOS diagnosed with Rotterdam criteria.
  • Age between 20 to 40-year-old
  • Undergoing frozen oocytes intracytoplasmic sperm injection transfer or frozen embryo transfer
  • Willingly accept to participate in the study

Exclusion Criteria:

  • Women > 40 years old or younger than 20.
  • Uterine pathology that decreases the chance of pregnancy or increases risk of miscarriage such as

    • Uterine fibroids (sub-mucous of any size or intramural of > 3 cm)
    • Uncontrolled endocrinal-pathological disease like

      • Cushing syndrome,
      • Adrenal hyperplasia,
      • Hyperprolactinemia,
      • Acromegaly,
      • Thyroid disease,
      • Diabetes mellitus, and
      • Immune disorders.
  • Presence of Hydrosalpinx
  • Not willing or able to sign the consent form.

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Experimental

    Active Comparator

    Arm Label

    PCOS women will receive letrozole ovarian stimulation.

    PCOS women will receive Estradiol and Progesterone (hormonal endometrial preparation).

    Arm Description

    Polycystic ovarian disease (PCOS) women undergoing frozen embryo transfer (FER) will use Letrozole 5 mg starting on day 3 of spontaneous menstrual period or after progesterone withdrawal bleeding for five consecutive days.

    PCOS women will use daily Cetorelix acetate 0.25 mg injections for 5 days from day 1-3 of the menstrual follow or after progesterone (P4) withdrawal bleeding. They will commence daily oral Estradiol Valerate (E2) 2 mg twice daily for 5 days starting from day 3 of the menstrual flow or after P4 withdrawal bleeding, then-after three times daily. When endometrial thickness reaches 7 mm or more, the dose of E2 will be reduced to 4 mg/ day. Women will start using vaginal micronized P4 100 mg three times daily starting from 8PM. After 48 hours of starting the vaginal P4, oral Dydrogesterone 10 mg three times daily will commence.

    Outcomes

    Primary Outcome Measures

    livebirth rate per embryo transfer
    A birth after 24 weeks gestation with a baby showing signs of life.

    Secondary Outcome Measures

    miscarriage rate per embryo transfer
    loss of pregnancy before 24 weeks gestation
    ongoing pregnancy per embryo transfer
    ongoing viable pregnancy (by ultrasound examination at 12 weeks' gestation)

    Full Information

    First Posted
    December 10, 2021
    Last Updated
    April 23, 2022
    Sponsor
    Dubai Fertility Center
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    1. Study Identification

    Unique Protocol Identification Number
    NCT05168865
    Brief Title
    Letrozole Versus Hormonal Preparation in Frozen Cycles of PCOS Patients.
    Official Title
    Letrozole Versus Hormonal Preparation in Frozen Cycles of PCOS Patients. Randomized Controlled Study
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    April 2022
    Overall Recruitment Status
    Not yet recruiting
    Study Start Date
    August 1, 2022 (Anticipated)
    Primary Completion Date
    February 1, 2024 (Anticipated)
    Study Completion Date
    April 1, 2024 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    Dubai Fertility Center

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No

    5. Study Description

    Brief Summary
    One of the indications of freezing is to reduce the risk of ovarian hyperstimulation syndrome particularly in polycystic ovarian disease (PCOS) women. Very few RCTs addressed the issue of optimizing the endometrium for a frozen cycle. Interestingly, Letrozole for ovarian stimulation showed significantly better reproductive outcome when compared with hormone replacement therapy (HRT) cycle. In addition, HRT cycle has been associated with higher miscarriage rate when compared with natural cycle frozen embryo transfer. Nevertheless, there is not yet a well-designed prospective randomized study comparing letrozole and HRT in PCOS women undergoing frozen embryo transfer.
    Detailed Description
    Freezing oocytes and embryos has become an integral part of the daily IVF practice. One of the indications of freezing is to reduce the risk of ovarian hyperstimulation syndrome particularly in polycystic ovarian disease (PCOS) women. Very few randomized control trials addressed the issue of optimizing the endometrium for a frozen cycle. As PCOS women do not regularly ovulate, most of their frozen cycles are conducted after hormonal replacement therapy (HRT) preparation of the endometrium or after ovulation induction. In HRT cycle the endometrium is prepared using exogenous estradiol and progesterone. While HRT cycles requires less monitoring and easy scheduling, it is costly, associated with increased risk of thrombosis and women must continue using the exogenous hormones up to 10 to 12 weeks of gestation. Interestingly, Letrozole for ovarian stimulation showed significantly better reproductive outcome when compared with HRT cycles. In agreement with the previous Chinese study, a retrospective Japanese ART registry data that included 110 722 frozen cycles confirmed the superiority of letrozole. Nevertheless, there is not yet a well-designed prospective randomized study. In addition, HRT cycle has been associated with higher miscarriage rate when compared with natural cycle frozen embryo transfer. HRT is usually used in patients with PCOS. A retrospective study including 2664 PCOS patients showed significant decrease in the pregnancy loss when letrozole was used when compared with HRT in frozen cycles. Investigators thought of comparing letrozole and HRT in women with PCOS who are undergoing frozen cycles in PCOS women. Live birth and miscarriage rates will be the primary outcomes.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Frozen Embryo Transfer, Polycystic Ovarian Disease, Letrozole, Hormone Replacement Therapy, Live Birth, Miscarriage

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Phase 4
    Interventional Study Model
    Parallel Assignment
    Masking
    None (Open Label)
    Allocation
    Randomized
    Enrollment
    236 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    PCOS women will receive letrozole ovarian stimulation.
    Arm Type
    Experimental
    Arm Description
    Polycystic ovarian disease (PCOS) women undergoing frozen embryo transfer (FER) will use Letrozole 5 mg starting on day 3 of spontaneous menstrual period or after progesterone withdrawal bleeding for five consecutive days.
    Arm Title
    PCOS women will receive Estradiol and Progesterone (hormonal endometrial preparation).
    Arm Type
    Active Comparator
    Arm Description
    PCOS women will use daily Cetorelix acetate 0.25 mg injections for 5 days from day 1-3 of the menstrual follow or after progesterone (P4) withdrawal bleeding. They will commence daily oral Estradiol Valerate (E2) 2 mg twice daily for 5 days starting from day 3 of the menstrual flow or after P4 withdrawal bleeding, then-after three times daily. When endometrial thickness reaches 7 mm or more, the dose of E2 will be reduced to 4 mg/ day. Women will start using vaginal micronized P4 100 mg three times daily starting from 8PM. After 48 hours of starting the vaginal P4, oral Dydrogesterone 10 mg three times daily will commence.
    Intervention Type
    Drug
    Intervention Name(s)
    Letrozole 2.5mg
    Other Intervention Name(s)
    estradiol and progesterone
    Intervention Description
    Letrozole 5 mg starting on day 3 of spontaneous menstrual period or after progesterone withdrawal bleeding for five consecutive days.
    Primary Outcome Measure Information:
    Title
    livebirth rate per embryo transfer
    Description
    A birth after 24 weeks gestation with a baby showing signs of life.
    Time Frame
    9 months
    Secondary Outcome Measure Information:
    Title
    miscarriage rate per embryo transfer
    Description
    loss of pregnancy before 24 weeks gestation
    Time Frame
    6 months
    Title
    ongoing pregnancy per embryo transfer
    Description
    ongoing viable pregnancy (by ultrasound examination at 12 weeks' gestation)
    Time Frame
    3 months

    10. Eligibility

    Sex
    Female
    Minimum Age & Unit of Time
    20 Years
    Maximum Age & Unit of Time
    40 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Women with PCOS diagnosed with Rotterdam criteria. Age between 20 to 40-year-old Undergoing frozen oocytes intracytoplasmic sperm injection transfer or frozen embryo transfer Willingly accept to participate in the study Exclusion Criteria: Women > 40 years old or younger than 20. Uterine pathology that decreases the chance of pregnancy or increases risk of miscarriage such as Uterine fibroids (sub-mucous of any size or intramural of > 3 cm) Uncontrolled endocrinal-pathological disease like Cushing syndrome, Adrenal hyperplasia, Hyperprolactinemia, Acromegaly, Thyroid disease, Diabetes mellitus, and Immune disorders. Presence of Hydrosalpinx Not willing or able to sign the consent form.

    12. IPD Sharing Statement

    Learn more about this trial

    Letrozole Versus Hormonal Preparation in Frozen Cycles of PCOS Patients.

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