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Frozen Embryo Transfer in Natural and Hormonal Replacement Cycles

Primary Purpose

Infertility

Status
Unknown status
Phase
Phase 3
Locations
Iran, Islamic Republic of
Study Type
Interventional
Intervention
frozen Embryo transfer
10,000U hCG injection
GnRH agonist (Superfact)
administration of 6 mg Estradiol valerate
Sponsored by
Royan Institute
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Infertility focused on measuring infertility froze emberyo transfer hormone replacement

Eligibility Criteria

20 Years - 37 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Patients with regular mensturation cycles
  2. Age 20-37 years
  3. Patients who underwent long protocol
  4. Body mass index (BMI) ≤ 30 kg/m2
  5. Patients who will undergo frozen embryo transfer for the first time

Exclusion Criteria:

  1. Oocyte or embryo donation cycles
  2. Uterine diseases or malformations
  3. Hyper prolactinemia
  4. Thyroid disorders
  5. Tuberculosis
  6. Recurrent abortion history
  7. Severe endometriosis
  8. Ovulation disorders

Sites / Locations

  • Royan InstituteRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Experimental

Experimental

Experimental

Experimental

Arm Label

Natural cycle

Natural cycle + hCG for ovulation induction

Hormonally controlled cycle with GnRH-a

Hormonally controlled cycle without GnRH-a

Arm Description

In natural cycle without hCG, daily monitoring of urinary LH is started from day eight of the cycle and frozen-thawed embryo transfer is planned 3-5 days after detection of LH surge, observing mature follicles in ultrasound and endometrial thickness over 7mm for cleavage embryos.

In natural cycle with hCG, after detection of mature follicles in ultrasound and endometrial thickness over 7mm, 10,000IU hCG is injected for ovulation and embryo transfer is performed 3-5 days later in cleavage stage.

In this group , injection of GnRH agonist (Superfact) at a subcutaneous daily dose of 0.5 mg is started on the day 17-19 of the natural menstrual cycle. Once pituitary desensitization is confirmed, hormonal treatment is commenced with 4mg/day oral Estradiol valerate and after 7 days if endometrial thickness is adequate, Estradiol administration will be continued with the same dose and 100mg Progesterone is administered before embryo transfer, otherwise patients are candidates for higher dosage of Estradiol till favourable endometrial thickness is achieved.

In the hormonal group without GnRH-a, endometrial preparation will be started with daily administration of 6 mg Estradiol valerate from the 2nd day of the natural menstrual cycle for 6 days. Then treatment will be continued similar to the 3rd group.

Outcomes

Primary Outcome Measures

Clinical pregnancy rate
The pregnancy rate will be evaluated in patients of each groups 4-6 weeks after embryo transfer.

Secondary Outcome Measures

Implantation rate
Evaluation the implantation rate in patients of each groups 4-6 weeks after frozen embryo transfer
chemical pregnancy rates
Evaluation the chemical pregnancy rates in patients of each group 2 weeks after embryo transfer.
Ongoing pregnancy
Evaluation the ongoing pregnancy in patients of each group 12 weeks after embryo transfer.
miscarriage rate
Evaluation the miscarriage rate in patients of each group 12 weeks after embryo transfer.

Full Information

First Posted
September 23, 2014
Last Updated
May 5, 2015
Sponsor
Royan Institute
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1. Study Identification

Unique Protocol Identification Number
NCT02251925
Brief Title
Frozen Embryo Transfer in Natural and Hormonal Replacement Cycles
Official Title
Comparison of Pregnancy Outcomes in Frozen Embryo Transfer in Natural and Hormonal Replacement Cycles: a Randomized Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
April 2012
Overall Recruitment Status
Unknown status
Study Start Date
September 2012 (undefined)
Primary Completion Date
October 2015 (Anticipated)
Study Completion Date
November 2015 (Anticipated)

3. Sponsor/Collaborators

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

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This study is a prospective randomized controlled trial to compare the pregnancy outcomes of frozen embryo transfer in natural and hormonal replacement cycles. The study population consisted of all infertile women with regular menstrual cycles who will undergo IVF/ICSI and frozen embryo transfer in Reproductive Biomedicine Research Center, Royan institute, Tehran Iran.
Detailed Description
In this study all patients who will undergo frozen embryo transfer are randomly allocated to be prepared for transfer by using either natural cycle (with or without hCG for ovulation induction) or Hormonal cycle (with or without administration of GnRH-a) In natural cycle without hCG, daily monitoring of urinary LH is started from day eight of the cycle and frozen-thawed embryo transfer is planned 3-5 days after detection of LH surge, observing mature follicles in ultrasound and endometrial thickness over 7mm for cleavage embryos. In natural cycle with hCG, after detection of mature follicles in ultrasound and endometrial thickness over 7mm, 10,000IU hCG is injected for ovulation and embryo transfer is performed 3-5 days later in cleavage stage. In group 3, injection of GnRH agonist (Superfact) at a subcutaneous daily dose of 0.5 mg is started on the day 17-19 of the natural menstrual cycle. Once pituitary desensitization is confirmed, hormonal treatment is commenced with 4mg/day oral Estradiol valerate and after 7 days if endometrial thickness is adequate, Estradiol administration will be continued with the same dose and 100mg Progesterone is administered before embryo transfer, otherwise patients are candidates for higher dosage of Estradiol till favourable endometrial thickness is achieved. In the hormonal group without GnRH-a, endometrial preparation will be started with daily administration of 6 mg Estradiol valerate from the 2nd day of the natural menstrual cycle for 6 days. Then treatment will be continued similar to the 3rd group.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Infertility
Keywords
infertility froze emberyo transfer hormone replacement

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
460 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Natural cycle
Arm Type
Experimental
Arm Description
In natural cycle without hCG, daily monitoring of urinary LH is started from day eight of the cycle and frozen-thawed embryo transfer is planned 3-5 days after detection of LH surge, observing mature follicles in ultrasound and endometrial thickness over 7mm for cleavage embryos.
Arm Title
Natural cycle + hCG for ovulation induction
Arm Type
Experimental
Arm Description
In natural cycle with hCG, after detection of mature follicles in ultrasound and endometrial thickness over 7mm, 10,000IU hCG is injected for ovulation and embryo transfer is performed 3-5 days later in cleavage stage.
Arm Title
Hormonally controlled cycle with GnRH-a
Arm Type
Experimental
Arm Description
In this group , injection of GnRH agonist (Superfact) at a subcutaneous daily dose of 0.5 mg is started on the day 17-19 of the natural menstrual cycle. Once pituitary desensitization is confirmed, hormonal treatment is commenced with 4mg/day oral Estradiol valerate and after 7 days if endometrial thickness is adequate, Estradiol administration will be continued with the same dose and 100mg Progesterone is administered before embryo transfer, otherwise patients are candidates for higher dosage of Estradiol till favourable endometrial thickness is achieved.
Arm Title
Hormonally controlled cycle without GnRH-a
Arm Type
Experimental
Arm Description
In the hormonal group without GnRH-a, endometrial preparation will be started with daily administration of 6 mg Estradiol valerate from the 2nd day of the natural menstrual cycle for 6 days. Then treatment will be continued similar to the 3rd group.
Intervention Type
Biological
Intervention Name(s)
frozen Embryo transfer
Intervention Description
In this study all patients who will undergo frozen embryo transfer are randomly allocated to be prepared for transfer by using either natural cycle (with or without hCG for ovulation induction) or Hormonal cycle (with or without administration of GnRH-a).
Intervention Type
Drug
Intervention Name(s)
10,000U hCG injection
Intervention Description
In natural cycle with hCG, after detection of mature follicles in ultrasound and endometrial thickness over 7mm, 10,000IU hCG is injected for ovulation and embryo transfer is performed 3-5 days later in cleavage stage.
Intervention Type
Drug
Intervention Name(s)
GnRH agonist (Superfact)
Intervention Description
In group 3, injection of GnRH agonist (Superfact) at a subcutaneous daily dose of 0.5 mg is started on the day 17-19 of the natural menstrual cycle. Once pituitary desensitization is confirmed, hormonal treatment is commenced with 4mg/day oral Estradiol valerate and after 7 days if endometrial thickness is adequate, Estradiol administration will be continued with the same dose and 100mg Progesterone is administered before embryo transfer, otherwise patients are candidates for higher dosage of Estradiol till favourable endometrial thickness is achieved.
Intervention Type
Drug
Intervention Name(s)
administration of 6 mg Estradiol valerate
Intervention Description
In the hormonal group without GnRH-a, endometrial preparation will be started with daily administration of 6 mg Estradiol valerate from the 2nd day of the natural menstrual cycle for 6 days. Then treatment will be continued similar to the 3rd group.
Primary Outcome Measure Information:
Title
Clinical pregnancy rate
Description
The pregnancy rate will be evaluated in patients of each groups 4-6 weeks after embryo transfer.
Time Frame
4 weeks
Secondary Outcome Measure Information:
Title
Implantation rate
Description
Evaluation the implantation rate in patients of each groups 4-6 weeks after frozen embryo transfer
Time Frame
4 weeks
Title
chemical pregnancy rates
Description
Evaluation the chemical pregnancy rates in patients of each group 2 weeks after embryo transfer.
Time Frame
2 weeks
Title
Ongoing pregnancy
Description
Evaluation the ongoing pregnancy in patients of each group 12 weeks after embryo transfer.
Time Frame
12 weeks
Title
miscarriage rate
Description
Evaluation the miscarriage rate in patients of each group 12 weeks after embryo transfer.
Time Frame
12 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
37 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients with regular mensturation cycles Age 20-37 years Patients who underwent long protocol Body mass index (BMI) ≤ 30 kg/m2 Patients who will undergo frozen embryo transfer for the first time Exclusion Criteria: Oocyte or embryo donation cycles Uterine diseases or malformations Hyper prolactinemia Thyroid disorders Tuberculosis Recurrent abortion history Severe endometriosis Ovulation disorders
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Nasser Aghdami, MD,PhD
Phone
(+98)23562000
Ext
516
Email
nasser.aghdami@royaninstitute.org
First Name & Middle Initial & Last Name or Official Title & Degree
Leila Arab, MD
Phone
(+98)23562000
Ext
414
Email
Leara91@gmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Hamid Gourabi, PhD
Organizational Affiliation
Head of Royan Institute
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Tahereh Madani, MD
Organizational Affiliation
Department of Endocrinology and Female Infertility at Reproductive Biomedicine Research Center, Royan Institute for Reproductive Biomedicine, ACECR, Tehran, Iran
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Ladan Mohammadi Yeganeh, MSC
Organizational Affiliation
Department of Endocrinology and Female Infertility at Reproductive Biomedicine Research Center, Royan Institute for Reproductive Biomedicine, ACECR, Tehran, Iran
Official's Role
Principal Investigator
Facility Information:
Facility Name
Royan Institute
City
Tehran
Country
Iran, Islamic Republic of
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Nasser Aghdami, MD,PhD
Phone
(+98)212356000
Ext
516
Email
nasser.aghdami@royaninstitute.org
First Name & Middle Initial & Last Name & Degree
Leila Arab, MD
Phone
(+98)23562000
Ext
414
Email
Leara91@gmail.com
First Name & Middle Initial & Last Name & Degree
Tahere Madani, MD
First Name & Middle Initial & Last Name & Degree
Ladan Mohammadi Yegane, MSC
First Name & Middle Initial & Last Name & Degree
Fariba Ramezani, MD
First Name & Middle Initial & Last Name & Degree
Mahnaz Rashidi, BSC
First Name & Middle Initial & Last Name & Degree
Narges Bagheri Lankarani, PhD
First Name & Middle Initial & Last Name & Degree
Fatemeh Hassani, MSC

12. IPD Sharing Statement

Citations:
PubMed Identifier
30707360
Citation
Madani T, Ramezanali F, Yahyaei A, Hasani F, Bagheri Lankarani N, Mohammadi Yeganeh L. Live birth rates after different endometrial preparation methods in frozen cleavage-stage embryo transfer cycles: a randomized controlled trial. Arch Gynecol Obstet. 2019 Apr;299(4):1185-1191. doi: 10.1007/s00404-019-05062-7. Epub 2019 Feb 1.
Results Reference
derived
Links:
URL
http://Royaninstitute.org
Description
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Frozen Embryo Transfer in Natural and Hormonal Replacement Cycles

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