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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT05632731
Other study ID # IRB-20220201-R
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date December 2022
Est. completion date December 2024

Study information

Verified date November 2022
Source Women's Hospital School Of Medicine Zhejiang University
Contact Yimin Zhu, Dr
Phone 0571-89992071
Email zhuyim@zju.edu.cn
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

In traditional assisted reproductive technology (ART), choosing multiple embryo transfer to get a high clinical pregnancy rate while increasing the risk of multiple pregnancies. Research showed that the single-cleavage embryo transfer could not simultaneously meet the dual requirements of maintaining pregnancy rate and reducing the multiple pregnancy rate.The purpose of this study was to observe the clinical outcome between double cleavage embryo transfers and single blastocyst transfers in fresh cycle through RCT study with GnRH antagonist protocol.


Description:

In traditional assisted reproductive technology (ART), choosing multiple embryo transfer to get a high clinical pregnancy rate while increasing the risk of multiple pregnancies. Research showed that in the fresh cleavage embryo transfer cycle, the clinical pregnancy rate increased with the increase of the number of high-quality embryos transferred, and so did the multiple pregnancy rate, suggesting that the single-cleavage embryo transfer could not simultaneously meet the dual requirements of maintaining pregnancy rate and reducing the multiple pregnancy rate. Compared with the embryo at cleavage stage, blastocyst culture is a process of survival of the fittest, which is physiologically more synchronized with endometrial development and can improve embryo implantation rate. The existing clinical research analysis is mostly limited to the down-regulating regimen, while the RCT study of high-quality with GnRH antagonist protocol is few. Therefore, the purpose of this study was to observe the clinical outcome between double cleavage embryo transfers and single blastocyst transfers in fresh cycle through RCT study with GnRH antagonist protocol.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 1236
Est. completion date December 2024
Est. primary completion date August 2024
Accepts healthy volunteers No
Gender Female
Age group 18 Years to 38 Years
Eligibility Inclusion Criteria: 1. patients with a diagnosis of primary or secondary infertility with a clinical indication for IVF/intracytoplasmic sperm injection (ICSI) 2. under 38 years of age 3. number of AFC=6, AMH>1.1ng/ml 4. no adverse factors of fresh embryo transplantation (evaluation by an experienced reproductive physician) 5. number of available embryos(day 3)=4 6. informed consent Exclusion Criteria: 1. PGT 2. with adenomyosis, endometrial compression by uterine fibroids, intrauterine adhesion, endometrial polyps and other factors unsuitable for fresh cycle transplantation

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
double cleavage-stage or single blastocyst stage embryos transfer
Infertile women requesting in vitro fertilization treatment were randomly assigned to undergo transfer of either two cleavage-stage embryos or a single blastocyst-stage embryo.

Locations

Country Name City State
n/a

Sponsors (2)

Lead Sponsor Collaborator
Women's Hospital School Of Medicine Zhejiang University ORGANON (SHANGHAI) PHARMACEUTICAL TECHNOLOGY CO., LTD.

Outcome

Type Measure Description Time frame Safety issue
Primary live birth rate per fresh transfer live birth, which was defined as the presence of a live fetus (or feti) after the 24th week of gestational age 2 year
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