- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04296357
Health of IVF Versus IVM Children (FM-BABIES) (FM-BABIES)
Follow-up of Children Born From In-vitro Maturation Versus In-vitro Fertilization: Follow-up of a Randomized Controlled Trial
Study Overview
Status
Conditions
Detailed Description
Since the birth of the first baby born from in-vitro maturation (IVM) in 1991, this technique has been considered an alternative solution for treating infertility beside conventional controlled ovarian stimulation for in-vitro fertilization (IVF). Since then, there are already more than 5000 children born from IVM, and that number is on the trend of increasing.
Regarding technique, immature oocytes (germinal vesicle - GV) were aspirated from secondary follicles sized from 2-10mm, under follicle-stimulating hormone (FSH) priming or no ovarian stimulation at all. Afterward, the maturation process was undertaken in an artificial medium, out of a living body. This technique, by reducing the usage of external hormones, is highly effective in minimizing the risk of ovarian hyperstimulation syndrome (OHSS) in women with high antral follicle count, especially polycystic ovarian syndrome, with a rate of OHSS recorded as low as 0 percent. Alongside that, the pregnancy rate, as well as the live birth rate of IVM, when proceeded well, is not lower than conventional IVF. Until now, there is only one randomized controlled trial comparing these two techniques directly.
Due to differences in the process of culturing between IVM and IVF, primarily the maturation is undertaken in an artificial medium, the health of children born from IVM received many interests. Numerous studies have been conducted to compare the development of children born from IVM and IVF. Neonatal outcomes of children born from IVM and IVF are considerably comparable. And the development of children born from these two techniques is not significantly different. All the information, as mentioned above, was not from randomized controlled trials but retrospective or prospective cohort studies. Thus, we conduct a follow up of our RCT to investigate the development of children born from IVM and IVM, to give strong evidence about the safety of IVM in women with high antral follicle count or especially PCOS.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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Ho Chi Minh City, Vietnam
- Mỹ Đức Hospital
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- All live babies born following the In-vitro Maturation and In-vitro fertilization from our FM study.
- Parents agree to participate in the study.
Exclusion Criteria:
- Babies died under or at 24 months
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
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IVF children
Children born from in-vitro fertilization
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Physical development and General health examination
Ages & Stages Questionnaires®, Third Edition (ASQ®-3) is a developmental screening tool designed for use by early educators and health care professionals.
It relies on parents as experts, is easy-to-use, family-friendly and creates the snapshot needed to catch delays and celebrate milestones.
Developmental Red flags Questionnaires
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IVM children
Children born from in-vitro maturation
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Physical development and General health examination
Ages & Stages Questionnaires®, Third Edition (ASQ®-3) is a developmental screening tool designed for use by early educators and health care professionals.
It relies on parents as experts, is easy-to-use, family-friendly and creates the snapshot needed to catch delays and celebrate milestones.
Developmental Red flags Questionnaires
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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The average total ASQ-3 score
Time Frame: Up to 24 months after birth
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ASQ-3 (Ages and Stages Questionaires®) has 5 aspects: Communication, Gross motor, Fine motor, Problem solving and Personal-Social Each aspect has 6 questions, if the answer is Yes, score = 10, Sometimes = 5 and Not yet = 0. ASQ-3 average = average score of 5 aspects. |
Up to 24 months after birth
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Duration of breast-feeding
Time Frame: Up to 24 months after birth
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Duration of breast-feeding
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Up to 24 months after birth
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Infant age at which weaning starts
Time Frame: Up to 24 months after birth
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Infant age at which weaning starts
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Up to 24 months after birth
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Number of hospital admission
Time Frame: Up to 24 months after birth
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Number of hospital admission
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Up to 24 months after birth
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Score of Communication
Time Frame: Up to 24 months after birth
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6 questions, if the answer is Yes, score = 10, Sometimes = 5 and Not yet = 0. Total score will be used: minimum = 0 and maximum = 60.
Each aspects in each stages has alternative threshold
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Up to 24 months after birth
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Score of Gross motor
Time Frame: Up to 24 months after birth
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6 questions, if the answer is Yes, score = 10, Sometimes = 5 and Not yet = 0. Total score will be used: minimum = 0 and maximum = 60.
Each aspects in each stages has alternative threshold
|
Up to 24 months after birth
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Score of Fine motor
Time Frame: Up to 24 months after birth
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6 questions, if the answer is Yes, score = 10, Sometimes = 5 and Not yet = 0. Total score will be used: minimum = 0 and maximum = 60.
Each aspects in each stages has alternative threshold
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Up to 24 months after birth
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Score of Problem solving
Time Frame: Up to 24 months after birth
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6 questions, if the answer is Yes, score = 10, Sometimes = 5 and Not yet = 0. Total score will be used: minimum = 0 and maximum = 60.
Each aspects in each stages has alternative threshold
|
Up to 24 months after birth
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Score of Personal-Social
Time Frame: Up to 24 months after birth
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6 questions, if the answer is Yes, score = 10, Sometimes = 5 and Not yet = 0. Total score will be used: minimum = 0 and maximum = 60.
Each aspects in each stages has alternative threshold
|
Up to 24 months after birth
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The rate of children who have at least one red flag sign
Time Frame: From 6 months to 24 months after birth
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He or she has at least one red flag sign by age For children at 6 months: he or she
For children at 12 months: he or she
For children at 24 months: he or she
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From 6 months to 24 months after birth
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Name of diseases that lead to hospital admission
Time Frame: Up to 24 months after birth
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Name of diseases that lead to hospital admission
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Up to 24 months after birth
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Weight
Time Frame: Up to 24 months after birth
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Weight on the examination date
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Up to 24 months after birth
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Height
Time Frame: Up to 24 months after birth
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Height on the examination date
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Up to 24 months after birth
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Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Gestational age at delivery
Time Frame: At birth
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Gestational age at delivery
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At birth
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Rate of congenital anomalies
Time Frame: At birth
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Any congenital anomalies detected in baby born
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At birth
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Mode of delivery
Time Frame: At birth
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Vaginal birth or C-section
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At birth
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Birth weight
Time Frame: At birth
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Weight of baby born
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At birth
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Head circumference
Time Frame: At birth
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Head circumference after birth
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At birth
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Rate of Periventricular haemorrhage
Time Frame: Up to 28 days after birth
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Periventricular haemorrhage II B or worse, will be diagnosed by repeated neonatal cranial ultrasound by the neonatologist according to the guidelines on neuro-imaging described by de Vries et al.
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Up to 28 days after birth
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Rate of Necrotizing enterocolitis
Time Frame: Up to 28 days after birth
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Necrotizing enterocolitis (NEC) will be diagnosed according to Bell.
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Up to 28 days after birth
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Rate of Proven sepsis
Time Frame: Up to 28 days after birth
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Proven sepsis, will be diagnosed on the combination of clinical signs and positive blood cultures.
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Up to 28 days after birth
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Rate of Composite of poor perinatal outcomes
Time Frame: Up to 28 days after birth
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Composite of poor perinatal outcomes, defined as intraventricular haemorrhage, respiratory distress syndrome, necrotizing enterocolitis or neonatal sepsis.
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Up to 28 days after birth
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Length of neonatal intensive care unit (NICU) admission
Time Frame: Up to 28 days after birth
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Number of admission days to NICU
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Up to 28 days after birth
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Rate of Respiratory distress syndrome
Time Frame: Up to 28 days after birth
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Respiratory distress syndrome (RDS), diagnosed as the presence of tachypnoea >60/minute, sternal recession and expiratory grunting, need for supplemental oxygen, and a radiological picture of diffuse reticulogranular shadowing with an air bronchogram
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Up to 28 days after birth
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Length circumference
Time Frame: At birth
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Head circumference after birth Head circumference after birth Head circumference after birth Length circumference after birth
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At birth
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The rate of long-term illness and chronic conditions
Time Frame: Up to 24 months after birth
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Any long-term illness and chronic condition appears in a child
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Up to 24 months after birth
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Collaborators and Investigators
Sponsor
Publications and helpful links
General Publications
- Vuong LN, Ho VNA, Ho TM, Dang VQ, Phung TH, Giang NH, Le AH, Pham TD, Wang R, Norman RJ, Smitz J, Gilchrist RB, Mol BW. Effectiveness and safety of in vitro maturation of oocytes versus in vitro fertilisation in women with high antral follicle count: study protocol for a randomised controlled trial. BMJ Open. 2018 Dec 9;8(12):e023413. doi: 10.1136/bmjopen-2018-023413.
- Cha KY, Koo JJ, Ko JJ, Choi DH, Han SY, Yoon TK. Pregnancy after in vitro fertilization of human follicular oocytes collected from nonstimulated cycles, their culture in vitro and their transfer in a donor oocyte program. Fertil Steril. 1991 Jan;55(1):109-13. doi: 10.1016/s0015-0282(16)54068-0.
- Das M, Son WY, Buckett W, Tulandi T, Holzer H. In-vitro maturation versus IVF with GnRH antagonist for women with polycystic ovary syndrome: treatment outcome and rates of ovarian hyperstimulation syndrome. Reprod Biomed Online. 2014 Nov;29(5):545-51. doi: 10.1016/j.rbmo.2014.07.019. Epub 2014 Aug 12.
- Gremeau AS, Andreadis N, Fatum M, Craig J, Turner K, McVeigh E, Child T. In vitro maturation or in vitro fertilization for women with polycystic ovaries? A case-control study of 194 treatment cycles. Fertil Steril. 2012 Aug;98(2):355-60. doi: 10.1016/j.fertnstert.2012.04.046. Epub 2012 May 31.
- Ho VNA, Braam SC, Pham TD, Mol BW, Vuong LN. The effectiveness and safety of in vitro maturation of oocytes versus in vitro fertilization in women with a high antral follicle count. Hum Reprod. 2019 Jun 4;34(6):1055-1064. doi: 10.1093/humrep/dez060.
- Mostinckx L, Segers I, Belva F, Buyl R, Santos-Ribeiro S, Blockeel C, Smitz J, Anckaert E, Tournaye H, De Vos M. Obstetric and neonatal outcome of ART in patients with polycystic ovary syndrome: IVM of oocytes versus controlled ovarian stimulation. Hum Reprod. 2019 Aug 1;34(8):1595-1607. doi: 10.1093/humrep/dez086.
- Roesner S, von Wolff M, Elsaesser M, Roesner K, Reuner G, Pietz J, Bruckner T, Strowitzki T. Two-year development of children conceived by IVM: a prospective controlled single-blinded study. Hum Reprod. 2017 Jun 1;32(6):1341-1350. doi: 10.1093/humrep/dex068.
- Sauerbrun-Cutler MT, Vega M, Keltz M, McGovern PG. In vitro maturation and its role in clinical assisted reproductive technology. Obstet Gynecol Surv. 2015 Jan;70(1):45-57. doi: 10.1097/OGX.0000000000000150.
- Shu-Chi M, Jiann-Loung H, Yu-Hung L, Tseng-Chen S, Ming-I L, Tsu-Fuh Y. Growth and development of children conceived by in-vitro maturation of human oocytes. Early Hum Dev. 2006 Oct;82(10):677-82. doi: 10.1016/j.earlhumdev.2006.01.012. Epub 2006 May 11.
- Yu EJ, Yoon TK, Lee WS, Park EA, Heo JY, Ko YK, Kim J. Obstetrical, neonatal, and long-term outcomes of children conceived from in vitro matured oocytes. Fertil Steril. 2019 Oct;112(4):691-699. doi: 10.1016/j.fertnstert.2019.05.034. Epub 2019 Jul 29.
- Vuong LN, Nguyen MHN, Nguyen NA, Ly TT, Tran VTT, Nguyen NT, Hoang HLT, Le XTH, Pham TD, Smitz JEJ, Mol BW, Norman RJ, Ho TM. Development of children born from IVM versus IVF: 2-year follow-up of a randomized controlled trial. Hum Reprod. 2022 Jul 30;37(8):1871-1879. doi: 10.1093/humrep/deac115.
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- CS/BVMĐ/20/05
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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