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Luteal Phase Support During Frozen Embryo Transfer Cycle

Primary Purpose

Infertility, Female, Frozen Embryo Transfer

Status
Completed
Phase
Phase 3
Locations
Iran, Islamic Republic of
Study Type
Interventional
Intervention
Strogen
Strogen
Sponsored by
Royan Institute
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Infertility, Female focused on measuring Ongoing pregnancy rate, Estrogen, Frozen embryo transfer, Luteal phase support

Eligibility Criteria

21 Years - 37 Years (Adult)FemaleAccepts Healthy Volunteers

Inclusion Criteria:

  1. Patients with surplus embryos undergone infertility treatment cycles (e.g. OHSS, inadequate endometrium, surplus frozen embryo from any cause)
  2. Age 21-37 years
  3. Normal BMI (18.5 <BMI <30)
  4. IVF / ICSI or IVF or ICSI cycles with antagonists or agonists protocols
  5. Frozen embryos on 2-3 days

Exclusion Criteria:

  1. Endometrial thickness ≤7mm
  2. Egg Donors
  3. Surrogacy
  4. Male factor infertility with azoospermia
  5. Age <37 years old
  6. Hydrosalpinx
  7. Uterine anomalies
  8. Myoma with a compression effect or submocusa myoma
  9. PGD
  10. Blastocyst embryo transfer, ZIFT and GIFT

Sites / Locations

  • Royan Institute

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

FET cycle, discontinue estradiol after 6 gestational weeks

FET cycle, continue estradiol till 12 gestational weeks

Arm Description

In patients 35 days after embryo transfer and observation of gestational sac with heart beat (6 weeks of pregnancy) by ultrasound, exogenous estrogen will discontinued while progesterone will remain daily use until twelfth week of pregnancy.

Control group receive 6 mg oral estrogen and 100 mg intramuscularly progesterone until 12 week of pregnancy.

Outcomes

Primary Outcome Measures

Ongoing pregnancy rate after frozen embryo transfer
Ongoing pregnancy was defined when the pregnancy had completed ≥20 weeks of gestation.

Secondary Outcome Measures

Maternal serum estrogen level
Maternal serum estrogen level
Maternal serum progesterone level
Maternal serum progesterone level

Full Information

First Posted
May 28, 2019
Last Updated
July 6, 2019
Sponsor
Royan Institute
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1. Study Identification

Unique Protocol Identification Number
NCT04013438
Brief Title
Luteal Phase Support During Frozen Embryo Transfer Cycle
Official Title
Duration of Estrogen for Luteal Phase in Pregnant Women Undergone Frozen Embryo Transfer Cycles- Randomized Controlled Trials Phase III
Study Type
Interventional

2. Study Status

Record Verification Date
May 2019
Overall Recruitment Status
Completed
Study Start Date
November 1, 2017 (Actual)
Primary Completion Date
January 1, 2019 (Actual)
Study Completion Date
April 30, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Royan Institute

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No

5. Study Description

Brief Summary
We aimed to decrease quantity of exogenous estrogen and evaluated the success rate of ongoing pregnancy in women undergone artificial FET who have a surplus embryos at previous fertility treatment cycles. In this study, endometrial prepared with standard long GnRH protocol and for luteal phase support patients received 6 mg oral E2 and intramuscularly P 100 mg/d and embryos on day 2-3 were transferred. Control group continued E2 until 12 week of pregnancy, while for cases after identify gestational sac with heart beat (the 6 week of pregnancy) by vaginal ultrasonography, E2 will discontinued.
Detailed Description
Approval Status: Confirmed Approval reference Number: IR.ACECR.ROYAN.REC.1395.70 Board Name: Ethics committee of Royan infertility institute Board Affiliation: Reza Samani Phone: +982122305236 Email: samani@royaninstitute.org Yes Health, Treatment and Medical Education Ministry: Iran Hormones replace therapy (Artificial) is a method for endometrium preparation and embryo transfer. In this protocol for decrease of spontaneous ovulation, exogenous estrogen began in 2-3 days on follicular phase of the menstrual cycle which continue about 10 to 14 days. In the following luteal phase support by progesterone begins on 14 to 16 days of cycles. The luteal phase is supported with different dose and duration of estradiol (E2) and progesterone (P) until 8-12 week of pregnancy. Studied reported a higher risk of thromboembolism in pregnant women that using exogenous estrogen. Also, excess estrogen might be resulted fetus congenital anomalies, low birth weight and increased susceptibility to breast cancer in female fetuses. On the other hands, it seems placenta in early pregnancy duration synthesize estrogen and this time estrogen sufficient as a product of progesterone metabolism. We aimed to decrease quantity of exogenous estrogen and evaluated the success rate of ongoing pregnancy in women undergone artificial FET who have a surplus embryos at previous fertility treatment cycles. In this study, endometrial prepared with standard long GnRH protocol and for luteal phase support patients received 6 mg oral E2 and intramuscularly P 100 mg/d and embryos on day 2-3 were transferred. Control group continued E2 until 12 week of pregnancy, while for cases after identify gestational sac with heart beat (the 6 week of pregnancy) by vaginal ultrasonography, E2 will discontinued. The level of maternal estrogen and progesterone measured at progesterone days (day 15), the day of embryo transfer, 6 and 12 weeks of pregnancy. This study is a randomized clinical trial to investigate the duration of estrogen for luteal phase in pregnant women undergone frozen embryo transfer cycles- Randomized controlled trials phase III. The study protocol is approved by the Ethics Committee (Institutional Review Board) of Royan institute and all participants provide informed consent.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Infertility, Female, Frozen Embryo Transfer
Keywords
Ongoing pregnancy rate, Estrogen, Frozen embryo transfer, Luteal phase support

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
60 (Actual)

8. Arms, Groups, and Interventions

Arm Title
FET cycle, discontinue estradiol after 6 gestational weeks
Arm Type
Experimental
Arm Description
In patients 35 days after embryo transfer and observation of gestational sac with heart beat (6 weeks of pregnancy) by ultrasound, exogenous estrogen will discontinued while progesterone will remain daily use until twelfth week of pregnancy.
Arm Title
FET cycle, continue estradiol till 12 gestational weeks
Arm Type
Active Comparator
Arm Description
Control group receive 6 mg oral estrogen and 100 mg intramuscularly progesterone until 12 week of pregnancy.
Intervention Type
Drug
Intervention Name(s)
Strogen
Other Intervention Name(s)
estradiol till 12 gestational weeks
Intervention Description
The OCP-LD begins in 2 to 3 days of the last menstrual cycle and then 500 μgr/d GnRH-a will received on day 17 for fourteen days. Then in 2-3 days of the next menstrual cycle, GnRH-a reduced to 200 μgr/d dose. the patients will receive 6 mg oral that will be continued for 14 days and during this time endometrium thickness evaluated by vaginal ultrasonography. If endometrial thickness is estimated ≥7mm, intramuscularly progesterone 100 mg/d will be started. After the onset of progesterone (days 17 to 18 cycles) frozen embryos transferred. Control group receive 6 mg oral estrogen and 100 mg intramuscularly progesterone until 12 week of pregnancy. The levels of maternal estrogen and progesterone was measured at the time of the starting day of progesterone (day 15), the day of embryo transfer, 6 and 12 weeks of pregnancy.
Intervention Type
Drug
Intervention Name(s)
Strogen
Other Intervention Name(s)
estradiol till 6 gestational weeks
Intervention Description
The OCP-LD begins in 2 to 3 days of the last menstrual cycle and then 500 μgr/d GnRH-a will received on day 17 for fourteen days. Then in 2-3 days of the next menstrual cycle, GnRH-a reduced to 200 μgr/d dose. the patients will receive 6 mg oral that will be continued for 14 days and during this time endometrium thickness evaluated by vaginal ultrasonography. If endometrial thickness is estimated ≥7mm, intramuscularly progesterone 100 mg/d will be started. After the onset of progesterone (days 17 to 18 cycles) frozen embryos transferred. In patients 35 days after embryo transfer and observation of gestational sac with heart beat (6 weeks of pregnancy) by ultrasound, exogenous estrogen will discontinued while progesterone will remain daily use until twelfth week of pregnancy. The levels of maternal estrogen and progesterone was measured at the time of the starting day of progesterone (day 15), the day of embryo transfer, 6 and 12 weeks of pregnancy.
Primary Outcome Measure Information:
Title
Ongoing pregnancy rate after frozen embryo transfer
Description
Ongoing pregnancy was defined when the pregnancy had completed ≥20 weeks of gestation.
Time Frame
≥20 weeks of gestational age
Secondary Outcome Measure Information:
Title
Maternal serum estrogen level
Description
Maternal serum estrogen level
Time Frame
The start day of using progesterone for luteal support in FET cycle (day 15 after onset estradiol), the day of embryo transfer (approximately 17-18 days after onset estradiol), 6 and 12 weeks of gestational age
Title
Maternal serum progesterone level
Description
Maternal serum progesterone level
Time Frame
The start day of using progesterone for luteal support in FET cycle (day 15 after onset estradiol), the day of embryo transfer (approximately 17-18 days after onset estradiol), 6 and 12 weeks of gestational age

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
21 Years
Maximum Age & Unit of Time
37 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Patients with surplus embryos undergone infertility treatment cycles (e.g. OHSS, inadequate endometrium, surplus frozen embryo from any cause) Age 21-37 years Normal BMI (18.5 <BMI <30) IVF / ICSI or IVF or ICSI cycles with antagonists or agonists protocols Frozen embryos on 2-3 days Exclusion Criteria: Endometrial thickness ≤7mm Egg Donors Surrogacy Male factor infertility with azoospermia Age <37 years old Hydrosalpinx Uterine anomalies Myoma with a compression effect or submocusa myoma PGD Blastocyst embryo transfer, ZIFT and GIFT
Facility Information:
Facility Name
Royan Institute
City
Tehran
Country
Iran, Islamic Republic of

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
34561715
Citation
Ghaffari F, Chekini Z, Vesali S. Duration of estradiol supplementation in luteal phase support for frozen embryo transfer in hormone replacement treatment cycles: a randomized, controlled phase III trial. Arch Gynecol Obstet. 2022 Mar;305(3):767-775. doi: 10.1007/s00404-021-06173-w. Epub 2021 Sep 24.
Results Reference
derived

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Luteal Phase Support During Frozen Embryo Transfer Cycle

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