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Progesterone Versus Progesterone Plus Dydrogesterone in FET (MiDRONE)

Primary Purpose

Infertility

Status
Completed
Phase
Not Applicable
Locations
Vietnam
Study Type
Interventional
Intervention
Micronized Progesterone
Micronized progesterone plus dydrogesterone
Sponsored by
Mỹ Đức Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Infertility focused on measuring FET, Micronized Progesterone, Dydrogesterone

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Undergoing frozen embryo transfer
  • Endometrial prepared by exogenous hormonal regimen
  • Permanent resident in Vietnam

Exclusion Criteria:

  • Having > 2 embryo transfer attempts
  • Having embryo(s) from donors cycles
  • Having embryo(s) from IVM
  • Having embryo(s) from PGT/PGS
  • Having endometrial abnormalities: polyp, sub-mucosal fibroid, cesarean scar defects, endometrial hyperplasia, endometrial fluid accumulation, endometrial adhesion.
  • Participating in another IVF study at the same time

Sites / Locations

  • Mỹ Đức Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

Micronized progesterone

Micronized progesterone plus dydrogesterone

Arm Description

Patients will receive micronized progesterone (Cyclogest® 400mg; Actavis) at the dose of 400mg twice daily (morning and evening).

Patients will receive micronized progesterone (Cyclogest® 400mg; Actavis) at the dose of 400mg twice daily (morning and evening) plus dydrogesterone (Duphaston® 10mg, Abbott) at the dose of 10mg twice daily (morning and evening).

Outcomes

Primary Outcome Measures

Live birth rate
The birth of at least one newborn after 24 weeks of gestation that exhibits any sign of life such as respiration, heartbeat, umbilical pulsation or movement of voluntary muscles (twin will be a single count).

Secondary Outcome Measures

The luteal progesterone level
The progesterone level in serum on day four after the progesterone application
The length of luteal phase
Starting on the day of progesterone application and ending on the last day prior menses
Positive pregnancy test rate
Serum human chorionic gonadotropin level greater than 5 mIU/mL after the completion of the first transfer
Clinical pregnancy rate
At least one gestational sac on ultrasound at 7 weeks' gestation with the detection of heart beat activity after the completion of the first transfer
Ongoing pregnancy rate
Pregnancy with detectable heart rate at 12 weeks' gestation or beyond after the completion of the first transfer.
Implantation rate rate
The number of gestational sacs per number of embryos transferred after the completion of the first transfer.
Ectopic pregnancy rate
A pregnancy in which implantation takes place outside the uterine cavity
Miscarriage rate
Pregnancy loss at < 12 weeks
Multiple pregnancy rate
Presence of more than one sac at early pregnancy ultrasound (6-8 weeks of gestation)
Gestational diabetes rate
A type of diabetes that develop during pregnancy
Hypertensive disorder of pregnancy rate
Comprising pregnancy induced hypertension (PIH); pre-eclampsia (PET) and eclampsia
Antepartum haemorrhage rate
Defined as bleeding from or in to the genital tract, occurring from 24 weeks of pregnancy and prior to the birth of the baby, including placenta previa, placenta accreta and unexplained
Preterm delivery rate
Defined as delivery at <24, <28, <32, <37 completed weeks
Birth weight (grams) of singletons and twins
Weight of baby born (grams)
Low birth weight rate
Weight of baby born < 2500 g at birth
Very low birth weight rate
Weight of baby born < 1500 g at birth
High birth weight rate
Weight of baby born >4000 gm at birth
Very high birth weight rate
Weight of baby born > 4500 gm at birth
Congenital anomaly diagnosed at birth rate
Any congenital anomalies detected in baby born
Venous thromboembolism (VTE) rate
Including deep venous thrombosis and pulmonary embolism
Gastrointestinal disorders rate
Including nausea, bloating, elevated liver enzymes
Nervous system disorders rate
Including headache, dizziness
Vaginal discharge rate
A fluid produced by glands in the vaginal wall and cervix that drains from the opening of the vagina
Vaginal discomfort rate
Including the symptoms of pain, itching, burning and swelling of vagina and vulva
Vulvovaginal pruritus rate
Itchiness of the vulva and vagina

Full Information

First Posted
June 17, 2019
Last Updated
February 22, 2021
Sponsor
Mỹ Đức Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT03998761
Brief Title
Progesterone Versus Progesterone Plus Dydrogesterone in FET
Acronym
MiDRONE
Official Title
Micronized Progesterone Versus Micronized Progesterone Plus Dydrogesterone for Luteal Phase Support in Frozen - Thawed Transfer: a Prospective Cohort Study
Study Type
Interventional

2. Study Status

Record Verification Date
February 2021
Overall Recruitment Status
Completed
Study Start Date
June 26, 2019 (Actual)
Primary Completion Date
January 5, 2021 (Actual)
Study Completion Date
January 31, 2021 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Mỹ Đức Hospital

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
Data Monitoring Committee
No

5. Study Description

Brief Summary
Frozen embryo transfer (FET) has been increasing important in IVF. Progesterone is essential for the endometrial secretory transformation, establishment and maintenance of pregnancy. In FET, as there is neither corpus luteum nor the support of hCG, the role of progesterone is even more important to ensure a sufficient luteal phase support. Vaginal progesterone has been the most common preparation for luteal support in fresh embryo transfer during IVF because of their ease of use and comparable effectiveness compared to intramuscular progesterone. Recently, there was evidence of the considerable variation in uptake, absorption and metabolism of intra-vaginal micronized progesterone. Dydrogesterone alone has described to have similar effectiveness, safety and tolerability prolfiles for luteal phase support compared to vaginal progesterone in luteal phase support for fresh embryo transfer. This prospective study compares the effectiveness of micronized progesterone versus micronized progesterone plus dydrogesterone for luteal phase support in FET.
Detailed Description
All patients undergoing FET will receive oral estradiol valerate (Valiera®; Laboratories Recalcine) 8 mg/day from the second or third day of menses for 6 days. Endometrial thickness will be monitored from day six onwards. From day 8-9 of menses, the estradiol dose could be adjusted from 8mg/day to 16mg/day according the development of the endometrium. Progesterone will be started when endometrial thickness reached 8 mm or more. In the first four months, all the patients will be treated with micronized progesterone. In five months later, the intervention will be changed to micronized progesterone plus dydrogesterone. In the second group of patients, the duration of study will be extended for one month due to the Lunar New Year holiday. Group 1: Micronized progesterone Patients will receive micronized progesterone (Cyclogest® 400mg; Actavis) at the dose of 400mg twice daily (morning and evening). Group 2: Micronized progesterone plus dydrogesterone Patients will receive micronized progesterone (Cyclogest® 400mg; Actavis) at the dose of 400mg twice daily (morning and evening) plus dydrogesterone (Duphaston 10mg) at the dose of 10mg twice daily (morning and evening). In both group, on the day of starting progesterone, the dose of estradiol will be decreased to 8mg/day. A maximum of 2 embryos will be thawed on the day of embryo transfer, which is four days or six days after the start of progesterone depending on day-3 or day-5 embryo transfer. After thawing, surviving embryos will be transferred into the uterus under ultrasound guidance. Estradiol and progesterone will be continued until the day of pregnancy test. If the pregnancy test is positive, the patients will continue to use 800 mg micronized progesterone or 800 mg micronized progesterone plus 20 mg dydrogestetrone, until 7 weeks of gestation. Blood samples will be obtained at day 4 after the use of progesterone. Serum progesterone will be measured. The blood tests will be taken in the morning, 2-3 h after the dydrogesterone and/or micronized progesterone application.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Infertility
Keywords
FET, Micronized Progesterone, Dydrogesterone

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
1364 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Micronized progesterone
Arm Type
Active Comparator
Arm Description
Patients will receive micronized progesterone (Cyclogest® 400mg; Actavis) at the dose of 400mg twice daily (morning and evening).
Arm Title
Micronized progesterone plus dydrogesterone
Arm Type
Active Comparator
Arm Description
Patients will receive micronized progesterone (Cyclogest® 400mg; Actavis) at the dose of 400mg twice daily (morning and evening) plus dydrogesterone (Duphaston® 10mg, Abbott) at the dose of 10mg twice daily (morning and evening).
Intervention Type
Drug
Intervention Name(s)
Micronized Progesterone
Other Intervention Name(s)
Cyclogest 400mg
Intervention Description
Progesterone will be started when endometrial thickness reached 8 mm or more. Patients will receive micronized progesterone (Cyclogest® 400mg; Actavis) at the dose of 400mg twice daily (morning and evening). A maximum of 2 embryos will be thawed on the day of embryo transfer, which is four days or six days after the start of progesterone depending on day-3 or day-5 embryo transfer. After thawing, surviving embryos will be transferred into the uterus under ultrasound guidance. Estradiol and progesterone will be continued until the day of pregnancy test. If the pregnancy test is positive, the patients will continue to use 800 mg micronized progesterone until 7 weeks of gestation.
Intervention Type
Drug
Intervention Name(s)
Micronized progesterone plus dydrogesterone
Other Intervention Name(s)
Cyclogest 400 mg + Duphaston 10 mg
Intervention Description
Progesterone will be started when endometrial thickness reached 8 mm or more. Patients will receive micronized progesterone (Cyclogest® 400mg; Actavis) at the dose of 400mg twice daily (morning and evening) plus dydrogesterone (Duphaston® 10mg, Abbott) at the dose of 10mg twice daily (morning and evening). A maximum of 2 embryos will be thawed on the day of embryo transfer, which is four days or six days after the start of progesterone depending on day-3 or day-5 embryo transfer. After thawing, surviving embryos will be transferred into the uterus under ultrasound guidance. Estradiol and progesterone will be continued until the day of pregnancy test. If the pregnancy test is positive, the patients will continue to use 800 mg micronized progesterone plus 20 mg dydrogestetrone until 7 weeks of gestation.
Primary Outcome Measure Information:
Title
Live birth rate
Description
The birth of at least one newborn after 24 weeks of gestation that exhibits any sign of life such as respiration, heartbeat, umbilical pulsation or movement of voluntary muscles (twin will be a single count).
Time Frame
At least 24 weeks of gestation up to the time of delivery
Secondary Outcome Measure Information:
Title
The luteal progesterone level
Description
The progesterone level in serum on day four after the progesterone application
Time Frame
On day four of the progesterone application
Title
The length of luteal phase
Description
Starting on the day of progesterone application and ending on the last day prior menses
Time Frame
On day sixteen of progesterone application
Title
Positive pregnancy test rate
Description
Serum human chorionic gonadotropin level greater than 5 mIU/mL after the completion of the first transfer
Time Frame
On day sixteen of progesterone application
Title
Clinical pregnancy rate
Description
At least one gestational sac on ultrasound at 7 weeks' gestation with the detection of heart beat activity after the completion of the first transfer
Time Frame
At 7 weeks of gestation
Title
Ongoing pregnancy rate
Description
Pregnancy with detectable heart rate at 12 weeks' gestation or beyond after the completion of the first transfer.
Time Frame
At 12 weeks' gestation
Title
Implantation rate rate
Description
The number of gestational sacs per number of embryos transferred after the completion of the first transfer.
Time Frame
At 3 weeks after embryo transferred
Title
Ectopic pregnancy rate
Description
A pregnancy in which implantation takes place outside the uterine cavity
Time Frame
At 12 weeks of gestation
Title
Miscarriage rate
Description
Pregnancy loss at < 12 weeks
Time Frame
At 12 weeks of gestation
Title
Multiple pregnancy rate
Description
Presence of more than one sac at early pregnancy ultrasound (6-8 weeks of gestation)
Time Frame
At 7 weeks' gestation
Title
Gestational diabetes rate
Description
A type of diabetes that develop during pregnancy
Time Frame
At 24 weeks of gestation
Title
Hypertensive disorder of pregnancy rate
Description
Comprising pregnancy induced hypertension (PIH); pre-eclampsia (PET) and eclampsia
Time Frame
From 20 weeks of gestation up to at birth
Title
Antepartum haemorrhage rate
Description
Defined as bleeding from or in to the genital tract, occurring from 24 weeks of pregnancy and prior to the birth of the baby, including placenta previa, placenta accreta and unexplained
Time Frame
From 24 weeks of gestation up to at birth
Title
Preterm delivery rate
Description
Defined as delivery at <24, <28, <32, <37 completed weeks
Time Frame
At birth
Title
Birth weight (grams) of singletons and twins
Description
Weight of baby born (grams)
Time Frame
At birth
Title
Low birth weight rate
Description
Weight of baby born < 2500 g at birth
Time Frame
At birth
Title
Very low birth weight rate
Description
Weight of baby born < 1500 g at birth
Time Frame
At birth
Title
High birth weight rate
Description
Weight of baby born >4000 gm at birth
Time Frame
At birth
Title
Very high birth weight rate
Description
Weight of baby born > 4500 gm at birth
Time Frame
At birth
Title
Congenital anomaly diagnosed at birth rate
Description
Any congenital anomalies detected in baby born
Time Frame
At birth
Title
Venous thromboembolism (VTE) rate
Description
Including deep venous thrombosis and pulmonary embolism
Time Frame
At 7 weeks of gestation
Title
Gastrointestinal disorders rate
Description
Including nausea, bloating, elevated liver enzymes
Time Frame
At 7 weeks of gestation
Title
Nervous system disorders rate
Description
Including headache, dizziness
Time Frame
At 7 weeks of gestation
Title
Vaginal discharge rate
Description
A fluid produced by glands in the vaginal wall and cervix that drains from the opening of the vagina
Time Frame
At 7 weeks of gestation
Title
Vaginal discomfort rate
Description
Including the symptoms of pain, itching, burning and swelling of vagina and vulva
Time Frame
At 7 weeks of gestation
Title
Vulvovaginal pruritus rate
Description
Itchiness of the vulva and vagina
Time Frame
At 7 weeks of gestation

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Undergoing frozen embryo transfer Endometrial prepared by exogenous hormonal regimen Permanent resident in Vietnam Exclusion Criteria: Having > 2 embryo transfer attempts Having embryo(s) from donors cycles Having embryo(s) from IVM Having embryo(s) from PGT/PGS Having endometrial abnormalities: polyp, sub-mucosal fibroid, cesarean scar defects, endometrial hyperplasia, endometrial fluid accumulation, endometrial adhesion. Participating in another IVF study at the same time
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Tuong M Ho, MD
Organizational Affiliation
Hope Research Center
Official's Role
Study Chair
Facility Information:
Facility Name
Mỹ Đức Hospital
City
Ho Chi Minh City
State/Province
Tan Binh
Country
Vietnam

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
26577241
Citation
Barbosa MW, Silva LR, Navarro PA, Ferriani RA, Nastri CO, Martins WP. Dydrogesterone vs progesterone for luteal-phase support: systematic review and meta-analysis of randomized controlled trials. Ultrasound Obstet Gynecol. 2016 Aug;48(2):161-70. doi: 10.1002/uog.15814. Epub 2016 Jul 8.
Results Reference
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PubMed Identifier
30304457
Citation
Griesinger G, Blockeel C, Sukhikh GT, Patki A, Dhorepatil B, Yang DZ, Chen ZJ, Kahler E, Pexman-Fieth C, Tournaye H. Oral dydrogesterone versus intravaginal micronized progesterone gel for luteal phase support in IVF: a randomized clinical trial. Hum Reprod. 2018 Dec 1;33(12):2212-2221. doi: 10.1093/humrep/dey306.
Results Reference
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PubMed Identifier
29778368
Citation
Griesinger G, Blockeel C, Tournaye H. Oral dydrogesterone for luteal phase support in fresh in vitro fertilization cycles: a new standard? Fertil Steril. 2018 May;109(5):756-762. doi: 10.1016/j.fertnstert.2018.03.034.
Results Reference
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PubMed Identifier
28333318
Citation
Tournaye H, Sukhikh GT, Kahler E, Griesinger G. A Phase III randomized controlled trial comparing the efficacy, safety and tolerability of oral dydrogesterone versus micronized vaginal progesterone for luteal support in in vitro fertilization. Hum Reprod. 2017 May 1;32(5):1019-1027. doi: 10.1093/humrep/dex023. Erratum In: Hum Reprod. 2017 Oct 1;32(10):2152.
Results Reference
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PubMed Identifier
26222435
Citation
Wang Y, He Y, Zhao X, Ji X, Hong Y, Wang Y, Zhu Q, Xu B, Sun Y. Crinone Gel for Luteal Phase Support in Frozen-Thawed Embryo Transfer Cycles: A Prospective Randomized Clinical Trial in the Chinese Population. PLoS One. 2015 Jul 29;10(7):e0133027. doi: 10.1371/journal.pone.0133027. eCollection 2015.
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Wei D, Liu JY, Sun Y, Shi Y, Zhang B, Liu JQ, Tan J, Liang X, Cao Y, Wang Z, Qin Y, Zhao H, Zhou Y, Ren H, Hao G, Ling X, Zhao J, Zhang Y, Qi X, Zhang L, Deng X, Chen X, Zhu Y, Wang X, Tian LF, Lv Q, Ma X, Zhang H, Legro RS, Chen ZJ. Frozen versus fresh single blastocyst transfer in ovulatory women: a multicentre, randomised controlled trial. Lancet. 2019 Mar 30;393(10178):1310-1318. doi: 10.1016/S0140-6736(18)32843-5. Epub 2019 Feb 28.
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Yanushpolsky E, Hurwitz S, Greenberg L, Racowsky C, Hornstein M. Crinone vaginal gel is equally effective and better tolerated than intramuscular progesterone for luteal phase support in in vitro fertilization-embryo transfer cycles: a prospective randomized study. Fertil Steril. 2010 Dec;94(7):2596-9. doi: 10.1016/j.fertnstert.2010.02.033. Epub 2010 Mar 27.
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Labarta E, Mariani G, Holtmann N, Celada P, Remohi J, Bosch E. Low serum progesterone on the day of embryo transfer is associated with a diminished ongoing pregnancy rate in oocyte donation cycles after artificial endometrial preparation: a prospective study. Hum Reprod. 2017 Dec 1;32(12):2437-2442. doi: 10.1093/humrep/dex316. Erratum In: Hum Reprod. 2018 Jan 1;33(1):178.
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Progesterone Versus Progesterone Plus Dydrogesterone in FET

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