Actively Recruiting
Development of IVF/ICSI Children Born From Different Endometrial Preparation Protocols
Led by Mỹ Đức Hospital · Updated on 2025-09-16
700
Participants Needed
1
Research Sites
172 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The efficacy and safety of endometrial preparation regimens remain controversial. In the most recent meta-analysis, using natural and modified natural cycle protocol to prepare the endometrium in frozen embryo transfer resulted in higher live birth rates. In addition, the natural cycle reduces the risk of gestational hypertension, postpartum haemorrhage, and extremely preterm delivery compared with regimens using exogenous hormones. Because there are many physiological and endocrinal differences in the frozen embryo transfer cycle with different endometrial preparation protocols, the development of children born from these regimens has received much attention. For example, there is a complete absence of the corpus luteum during the cycle of exogenous hormone administration. Or in the modified natural cycle, the pharmacokinetics is not entirely the same as the natural physiology when using an additional ovulatory injection with hCG. To date, there have been no longitudinal follow-up studies that evaluated and compared the long-term development of IVF/ICSI children born from frozen embryo transfer with different endometrial preparation protocols. Thus, the investigators conduct a follow-up of our RCT to investigate the IVF/ICSI children born from frozen embryo transfer with different endometrial preparation protocols to give strong evidence about the safety of the three most common endometrial preparation protocols in women undergoing frozen embryo transfer.
CONDITIONS
Official Title
Development of IVF/ICSI Children Born From Different Endometrial Preparation Protocols
Who Can Participate
Eligibility Criteria
You may qualify if you...
- All live IVF/ICSI babies born from frozen embryo transfer following the natural cycle, modified natural cycle, and artificial cycle from MONART study
- Parents agree to participate in the study.
You will not qualify if you...
- Babies who died at or before 24 months of age
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
My Duc Hospital
Ho Chi Minh City, Vietnam, 70000
Actively Recruiting
Research Team
H
Hieu LT Hoang
CONTACT
V
Vu NA Ho
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
3
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