Comparison of Clinical Outcomes in Fresh Cycle With Single Blastocyst Stage and Double Cleavage-stage Embryos: a Single-center, Non-blind, Randomized Controlled Study

Sponsor
Women's Hospital School Of Medicine Zhejiang University (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05632731
Collaborator
ORGANON (SHANGHAI) PHARMACEUTICAL TECHNOLOGY CO., LTD. (Other)
1,236
2
24

Study Details

Study Description

Brief 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.

Condition or Disease Intervention/Treatment Phase
  • Procedure: double cleavage-stage or single blastocyst stage embryos transfer
N/A

Detailed 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.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
1236 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Double (Participant, Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
Comparison of Clinical Outcomes in Fresh Cycle With Single Blastocyst Stage and Double Cleavage-stage Embryos: a Single-center, Non-blind, Randomized Controlled Study
Anticipated Study Start Date :
Dec 1, 2022
Anticipated Primary Completion Date :
Aug 1, 2024
Anticipated Study Completion Date :
Dec 1, 2024

Arms and Interventions

Arm Intervention/Treatment
Other: Double Cleavage-stage Embryos transfer

In group A, two embryos at cleavage stage were transplanted on the third day after oocyte retrieval.

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.

Other: Single Blastocyst Stage Embryos transfer

Group B was graded by Gardner blastocyst grading method, and one blastocyst was transplanted on the 5th or 6th day after oocyte retrieval.

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.

Outcome Measures

Primary Outcome Measures

  1. live birth rate per fresh transfer [2 year]

    live birth, which was defined as the presence of a live fetus (or feti) after the 24th week of gestational age

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 38 Years
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
No
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

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

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

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Women's Hospital School Of Medicine Zhejiang University
ClinicalTrials.gov Identifier:
NCT05632731
Other Study ID Numbers:
  • IRB-20220201-R
First Posted:
Dec 1, 2022
Last Update Posted:
Dec 1, 2022
Last Verified:
Nov 1, 2022
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Dec 1, 2022