Health of IVF Versus IVM Children (FM-BABIES) (FM-BABIES)

February 12, 2022 updated by: Mỹ Đức Hospital

Follow-up of Children Born From In-vitro Maturation Versus In-vitro Fertilization: Follow-up of a Randomized Controlled Trial

The investigators conduct a follow up of our randomized controlled trial (RCT) to investigate the development of children born from In-vitro fertilization (IVF) and In-vitro maturation (IVM), in order to give strong evidence about the safety of IVM in women with high antral follicle count or especially polycystic ovary syndrome (PCOS).

Study Overview

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

Observational

Enrollment (Actual)

231

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Ho Chi Minh City, Vietnam
        • Mỹ Đức Hospital

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

6 months to 2 years (Child)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

Live babies born following the IVF and IVM from our FM study (NCT03405701)

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

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
IVF children
Children born from in-vitro fertilization
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
IVM children
Children born from in-vitro maturation
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

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
The average total ASQ-3 score
Time Frame: Up to 24 months after birth

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

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Duration of breast-feeding
Time Frame: Up to 24 months after birth
Duration of breast-feeding
Up to 24 months after birth
Infant age at which weaning starts
Time Frame: Up to 24 months after birth
Infant age at which weaning starts
Up to 24 months after birth
Number of hospital admission
Time Frame: Up to 24 months after birth
Number of hospital admission
Up to 24 months after birth
Score of Communication
Time Frame: Up to 24 months after birth
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
Score of Gross motor
Time Frame: Up to 24 months after birth
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
Score of Fine motor
Time Frame: Up to 24 months after birth
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
Score of Problem solving
Time Frame: Up to 24 months after birth
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
Score of Personal-Social
Time Frame: Up to 24 months after birth
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
The rate of children who have at least one red flag sign
Time Frame: From 6 months to 24 months after birth

He or she has at least one red flag sign by age For children at 6 months: he or she

  • Do not know to flip before 3 months
  • Still holding hands constantly at 3 months
  • Do not pay attention to the stimulation from the environment
  • Poor head control
  • No access to objects/ toys before 5 months
  • No laughter

For children at 12 months: he or she

  • No babbling before 6 months
  • Unable to sit down in a W-style at 7 months
  • Unable to identify audio source before 10 months
  • Still holding things in your mouth often for 12 months

For children at 24 months: he or she

  • Do not speak consonants before 15 months
  • Do not know imitate before 16 months
  • Do not know to point fingers to attract attention about objects that he or she cares about
  • Show right-handedness before 18 months
  • Unable to ascend and descend stairs at 24 months
  • Repeat the machinery of others' words
  • Not reached the single 50 marks yet by 24 months
From 6 months to 24 months after birth
Name of diseases that lead to hospital admission
Time Frame: Up to 24 months after birth
Name of diseases that lead to hospital admission
Up to 24 months after birth
Weight
Time Frame: Up to 24 months after birth
Weight on the examination date
Up to 24 months after birth
Height
Time Frame: Up to 24 months after birth
Height on the examination date
Up to 24 months after birth

Other Outcome Measures

Outcome Measure
Measure Description
Time Frame
Gestational age at delivery
Time Frame: At birth
Gestational age at delivery
At birth
Rate of congenital anomalies
Time Frame: At birth
Any congenital anomalies detected in baby born
At birth
Mode of delivery
Time Frame: At birth
Vaginal birth or C-section
At birth
Birth weight
Time Frame: At birth
Weight of baby born
At birth
Head circumference
Time Frame: At birth
Head circumference after birth
At birth
Rate of Periventricular haemorrhage
Time Frame: Up to 28 days after birth
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.
Up to 28 days after birth
Rate of Necrotizing enterocolitis
Time Frame: Up to 28 days after birth
Necrotizing enterocolitis (NEC) will be diagnosed according to Bell.
Up to 28 days after birth
Rate of Proven sepsis
Time Frame: Up to 28 days after birth
Proven sepsis, will be diagnosed on the combination of clinical signs and positive blood cultures.
Up to 28 days after birth
Rate of Composite of poor perinatal outcomes
Time Frame: Up to 28 days after birth
Composite of poor perinatal outcomes, defined as intraventricular haemorrhage, respiratory distress syndrome, necrotizing enterocolitis or neonatal sepsis.
Up to 28 days after birth
Length of neonatal intensive care unit (NICU) admission
Time Frame: Up to 28 days after birth
Number of admission days to NICU
Up to 28 days after birth
Rate of Respiratory distress syndrome
Time Frame: Up to 28 days after birth
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
Up to 28 days after birth
Length circumference
Time Frame: At birth
Head circumference after birth Head circumference after birth Head circumference after birth Length circumference after birth
At birth
The rate of long-term illness and chronic conditions
Time Frame: Up to 24 months after birth
Any long-term illness and chronic condition appears in a child
Up to 24 months after birth

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

March 1, 2020

Primary Completion (Actual)

January 5, 2022

Study Completion (Actual)

January 5, 2022

Study Registration Dates

First Submitted

March 3, 2020

First Submitted That Met QC Criteria

March 4, 2020

First Posted (Actual)

March 5, 2020

Study Record Updates

Last Update Posted (Actual)

February 15, 2022

Last Update Submitted That Met QC Criteria

February 12, 2022

Last Verified

February 1, 2022

More Information

Terms related to this study

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)?

UNDECIDED

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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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