MONART: Natural Cycle vs. Modified Natural Cycle vs. Artificial Cycle Protocol for Endometrial Preparation.
Study Details
Study Description
Brief Summary
Fresh embryo transfer is a routine procedure in vitro fertilization (IVF) treatment. Since the first live birth after an IVF-FET (frozen embryo transfer), recent years have seen a dramatic rise in the number of FET cycles. Three endometrial preparation protocols for frozen-thawed embryo transfer, including artificial, natural, modified natural protocol, have been studied and applied to maximize treatment outcomes. However, those methods are being applied empirically as their efficacy and safety are yet to be determined. The objective of this study is to compare the effectiveness and safety of those protocols.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
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N/A |
Detailed Description
This trial will be conducted at My Duc Hospital, Ho Chi Minh City, Viet Nam. Women who are potentially eligible will be provided information about the trial as long as their stimulation cycles are initiated. Screening for eligibility will be performed by treating physicians on day 2 of the menstrual cycle in the subsequent frozen embryo transfer cycles. Patients will be provided a copy of the informed consent documents. Written informed consent is going to be obtained by the investigator from all women before the enrolment. Women will be randomized (1:1:1) to AC (artificial cycle) or NC (natural cycle) or mNC (modified natural cycle) protocols using block randomization with a variable block size of 6 or 9 by an independent study coordinator via telephone, using a computer-generated random list (block size of 6, or 9).
Artificial protocol The endometrium is prepared using oral estradiol valerate (Valiera®; Laboratories Recalcine) 8 mg/day, ranging from the second or fourth menstruation day. The endometrial thickness will be monitored from day six onwards, and vaginal progesterone (Utrogestan®; Besins) 800 mg/day will be initiated when endometrial thickness reaches ≥7 mm. Estradiol exposure must be lasting for ≥9 days before progesterone administration. Embryo transfer will be scheduled by the time of the initiation of progesterone and embryo stages. In cases where a dominant follicle emerged, serum LH and progesterone will be determined to rule out luteinization. If LH concentrations are <13 IU and progesterone levels <7 nmol/l, luteinization will deem not to have occurred, and FET was performed.
Natural protocol The first ultrasound scan will be performed on the second to the fourth day of the menstrual cycle to identify any problem related to the patients' uterus or adnexa. The second ultrasound will be performed on the sixth day of the cycle. Daily ultrasound and serum estradiol and LH level evaluation will be performed when the mean diameter of the dominant follicle of ≥14 mm. LH surge initiation is defined as a concentration of 180% above the latest serum value available in that patient with a continued rise thereafter to a level of 20 IU/l or more detected by the ECLIA method (Roche Cobas® E 801, Roche Diagnostics, Germany). Embryo transfer will be scheduled by the time of the initiation of LH and embryo stages.
modified Natural protocol The first ultrasound scan will be performed on the second to the fourth day of the menstrual cycle to identify any problem related to patients' uterus or adnexa. A second ultrasound scan will be performed on the sixth day of the cycle; if there is at least one follicle with a diameter of ≥12 mm, an ultrasound scan will be performed daily. When the dominant follicle's mean diameter is ≥16 mm, human chorionic gonadotropin - hCG (Ovitrelle® 250 μg; Merck, Kenilworth, NJ, USA) will be injected to trigger ovulation. Embryo transfer will be scheduled by the time of the hCG injection and embryo stages.
Cycle cancellation
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Artificial protocol: When the endometrial thickness is below 7mm after a duration of estradiol administration of ≥21 days or the emerging of a dominant follicle.
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Natural cycle protocol: When there is no onset of LH surge observed after a duration of ≥21 days.
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modified Natural cycle protocol: When there is no dominant follicle with a diameter of 16mm emerged after a duration of ≥21 days.
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Both protocols: When there is no embryo survived after thawing. Frozen embryo transfer A maximum of 2 day-3 and one day-5 embryo will be thawed on the day of embryo transfer, three days after the start of progesterone. Two hours after thawing, surviving embryos will be transferred into the uterus under ultrasound guidance using a soft uterine catheter (Gynétics®, Belgium).
A series of progesterone levels evaluation will be performed at three times: (1) The start of the cycle, (2) Before the time the embryo transfer is scheduled, (3) On the day of embryo transfer.
The blood sample at the start of the cycle will be stored for further epigenetics analysis.
Future babies' health will also be performed separately.
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Active Comparator: NC (Natural cycle) Performing the first ultrasound scan will be performed on the second to the fourth day of the menstrual cycle to identify any problem related to the patients' uterus or adnexa. The second ultrasound will be performed on the sixth day of the cycle. Daily ultrasound and serum estradiol and LH level evaluation will be performed when the mean diameter of the dominant follicle of ≥14 mm. LH surge initiation is defined as a concentration of 180% above the latest serum value available in that patient with a continued rise thereafter to a level of 20 IU/l or more detected by the ECLIA method (Roche Cobas® E 801, Roche Diagnostics, Germany). Embryo transfer will be scheduled by the time of the initiation of LH and embryo stages. |
Procedure: NC
The first ultrasound scan will be performed on the second to the fourth day of the menstrual cycle to identify any problem related to the patients' uterus or adnexa. The second ultrasound will be performed on the sixth day of the cycle. Daily ultrasound and serum estradiol and LH level evaluation will be performed when the mean diameter of the dominant follicle of ≥14 mm. LH surge initiation is defined as a concentration of 180% above the latest serum value available in that patient with a continued rise thereafter9 to a level of 20 IU/l or more10 detected by the ECLIA method (Roche Cobas® E 801, Roche Diagnostics, Germany). Embryo transfer will be scheduled by the time of the initiation of LH and embryo stages.
|
| Active Comparator: mMC (modified Natural cycle) Performing the first ultrasound scan on the second to the fourth day of the menstrual cycle to identify any problem related to patients' uterus or adnexa. A second ultrasound scan will be performed on the sixth day of the cycle; if there is at least one follicle with a diameter of ≥12 mm, an ultrasound scan will be performed daily. When the dominant follicle's mean diameter is ≥16 mm, human chorionic gonadotropin (Ovitrelle® 250 μg; Merck, Kenilworth, NJ, USA) will be injected to trigger ovulation. Embryo transfer will be scheduled by the time of the hCG injection and embryo stages. |
Procedure: mNC
The first ultrasound scan will be performed on the second to the fourth day of the menstrual cycle to identify any problem related to patients' uterus or adnexa. A second ultrasound scan will be performed on the sixth day of the cycle; if there is at least one follicle with a diameter of ≥12 mm, an ultrasound scan will be performed daily. When the dominant follicle's mean diameter is ≥16 mm, human chorionic gonadotropin (Ovitrelle® 250 μg; Merck, Kenilworth, NJ, USA) will be injected to trigger ovulation. Embryo transfer will be scheduled by the time of the hCG injection and embryo stages.
|
| Active Comparator: AC (Artificial cycle) Preparing the endometrium by using oral estradiol valerate (Valiera®; Laboratories Recalcine) 8 mg/day, ranging from the second or fourth menstruation day. The endometrial thickness will be monitored from day six onwards, and vaginal progesterone (Utrogestan®; Besins) 800 mg/day will be initiated when endometrial thickness reaches ≥7 mm. Estradiol exposure must be lasting for ≥9 days before progesterone administration. Embryo transfer will be scheduled by the time of the initiation of progesterone and embryo stages. |
Procedure: AC
The endometrium is prepared using oral estradiol valerate (Valiera®; Laboratories Recalcine) 8 mg/day, ranging from the second or fourth menstruation day. The endometrial thickness will be monitored from day six onwards, and vaginal progesterone (Utrogestan®; Besins) 800 mg/day will be initiated when endometrial thickness reaches ≥7 mm. Estradiol exposure must be lasting for ≥9 days before progesterone administration. Embryo transfer will be scheduled by the time of the initiation of progesterone and embryo stages.
|
Outcome Measures
Primary Outcome Measures
- Live birth rate after one frozen embryo transfer cycle [At 24 weeks of gestation]
Live birth is defined as the complete expulsion or extraction from a woman of a product of fertilisation, after 24 completed weeks of gestational age; which, after such separation, breathes or shows any other evidence of life, such as heart beat, umbilical cord pulsation or definite movement of voluntary muscles, irrespective of whether the umbilical cord has been cut or the placenta is attached. A birth weight of 350 grams or more can be used if gestational age is unknown (twins are a single count).
Secondary Outcome Measures
- Positive pregnancy test [At 2 weeks after embryo placement]
Serum ß-hCG ≥25mIU/mL
- Clinical pregnancy [At 5 weeks after embryo placement]
Having at least 1 gestational sac on ultrasound at 5 weeks' gestation
- Ongoing pregnancy [At 10 weeks after embryo placement]
Having at least 1 gestational sac on ultrasound at 12 weeks' gestation with heart beat activity
- Implantation [At 3 weeks after embryo placement]
Implantation rate is explained as as the number of gestational sacs per number of embryos transferred.
- Ectopic pregnancy [At 12 weeks of gestation]
A pregnancy outside the uterine cavity, diagnosed by ultrasound, surgical visualisation, or histopathology
- Miscarriage [At 20 weeks of gestation]
The spontaneous loss of an intra-uterine pregnancy prior to 20 completed weeks of gestational age
- Preterm delivery [At 22, 28, 32 weeks and 37 weeks of gestation]
Multiple definitions, defined as delivery at <24, <28, <32, <37 completed weeks
- Endometrial preparation cycles cancelation [At 4 weeks from the start of treatment cycle]
Cycle cancelling due to: No follicular development or no LH surge initiation in NC group Cycles with unfavorable endometrium before ovulation or addition of progesterone: endometrial thickness <7mm after 12 days taking estradiol valerate Fluid in cavity Side effects of taking exogenous hormones: severe migraine/headache, mood swings, vaginal bleeding, nausea; venous thromboembolism, stroke. Patient preferences
- Gestational diabetes mellitus [At 24 to 28 weeks of gestation]
using a 75g oral glucose tolerance test
- Hypertensive disorders of pregnancy [At 20 weeks of gestation or beyond after the completion of the first transfer]
Pregnancy-induced hypertension, pre-eclampsia and eclampsia
- Birth weight [At the time of delivery]
Weight of singletons and twins
- Low birth weight [At birth]
Weight < 2500 gm at birth
- Very low birth weight [At birth]
Weight < 1500 gm at birth
- High birth weight [At birth]
Weight >4000 gm at birth
- Very high birth weight [At birth]
Weight >4500 gm at birth
- Major congenital abnormalities [At birth]
Structural, functional, and genetic anomalies, that occur during pregnancy, and identified antenatally, at birth, or later in life, and require surgical repair of a defect, or are visually evident, or are life-threatening, or cause death. Any congenital anomaly will be included as followed definition of congenital abnormalities in Surveillance of Congenital Anomalies by Division of Birth Defects and Developmental Disabilities, NCBDDD, Centers for Disease Control and Prevention (2020).
- Admission to NICU [At birth]
The admittance of the newborn to NICU
- Venous thromboembolism relating to medication [From the start of treatment up to 10 weeks of gestation]
Venous thromboembolism is diagnosed after clinical examination, ultrasound scan and blood test
- Multiple pregnancy [At 6 to 8 weeks' gestation]
≥1 gestational sac at early pregnancy ultrasound
- Multiple delivery [At 24 weeks' gestation]
Birth of more than one baby beyond 24 weeks
- Cost-effectiveness [Two year after randomization]
Including direct and indirect costs; costs related to complications treatment. Cost data will be collected for a supplementary analysis and will be reported in a separated paper.
- Still birth [At 20 weeks' gestation]
The death of a fetus prior to the complete expulsion or extraction from its mother after 20 completed weeks of gestational age. The death is determined by the fact that, after such separation, the fetus does not breathe or show any other evidence of life, such as heartbeat, umbilical cord pulsation, or definite movement of voluntary muscles.
Eligibility Criteria
Criteria
Inclusion Criteria:
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Aged of 18 to 45
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Having menstrual cycle duration of 24 to 38 days
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Undergoing no more than 3 previous IVF/ICSI - FET cycles
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Planning a frozen-thawed embryo transfer
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Agreeing to have no more than 2 day 3 and 1 day 5 embryos transferred
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Not participating in another IVF study at the same time
Exclusion Criteria:
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Menopausal/ Anovulatory women
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Having contraindication for exogenous hormones administration: breast cancer, risks of venous thromboembolism
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Having embryos from in vitro Maturation or oocyte donation or PGT (pre-implantation genetics testings) cycles
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Having uterine abnormalities (e.g., adenomyosis, intrauterine adhesions, unicornuate/ bicornuate/ arcuate uterus; unremoved hydrosalpinx, endometrial polyp)
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | My Duc Hospital | Ho Chi Minh City | Vietnam |
Sponsors and Collaborators
- Mỹ Đức Hospital
- University of Medicine and Pharmacy at Ho Chi Minh City
Investigators
- Principal Investigator: Lan N Vuong, MD, PhD, University of Medicine and Pharmacy at Ho Chi Minh City
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- 187/HĐĐĐ-ĐHYD