A Study of Preimplantation Genetic Screening With Next Generation Sequencing Technology on Advanced Age Women
A Prospective Randomized Controlled Study of Preimplantation Genetic Screening With Next Generation Sequencing Technology on Advanced Age Women
1 other identifier
interventional
124
1 country
1
Brief Summary
With the development of society, more and more aged pregnant women because of various reasons, their abnormality rate of egg chromosome was higher than that of young women, then the abnormality rate of embryo chromosome is higher too, so the pregnancy rate in aged women is lower, abortion rate is higher. In order to improve the pregnancy rate in aged women, cut down their abortion rate 、fetal birth with abnormal chromosome, and the risk of pregnancy termination after the prenatal diagnosis, reduce their pain of body and mind, the investigators will carry out this study. This is a prospective randomized controlled study of preimplantation genetic screening with Next generation sequencing technology. The embryos with more developmental potential and normal chromosomes should be selected. There is no related studies in Chinese. Most international research are limited to fluorescence in situ hybridization (FISH) technique, not on the embryo chromosome comprehensive screening. So there is no evidence of the effects of PGS on advanced age women. This study is to compare the outcomes between the advanced age women with two methods respectively. After blastocyst culture, blastocysts will be transferred in the control group. In the Preimplantation Genetic Screening (PGS) group, blastocyst embryo trophoblast biopsy will be performed and chromosome screening with Next generation sequencing(NGS) technology, at the same time, the blastocysts will be frozen, then the blastocysts with normal chromosome will be thawed and transferred. The investigators expect that, in PGS group live birth rate 、cancellation rate and pregnancy rate are higher than in control group; abortion rate is lower than that of the control group.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Sep 2016
Typical duration for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
August 10, 2016
CompletedFirst Posted
Study publicly available on registry
August 16, 2016
CompletedStudy Start
First participant enrolled
September 23, 2016
CompletedPrimary Completion
Last participant's last visit for primary outcome
May 1, 2018
CompletedStudy Completion
Last participant's last visit for all outcomes
August 1, 2019
CompletedJanuary 26, 2022
March 1, 2020
1.6 years
August 10, 2016
January 10, 2022
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
live birth rate
At birth
Secondary Outcomes (3)
cancellation rate
Up to the day of embryo transferred
Pregnancy Rate
Up to 28th day after embryo transferred
abortion rate
Through pregnancy period,average 10 months
Study Arms (2)
PGS group
EXPERIMENTALAfter blastocyst culture, blastocyst embryo trophoblast biopsy will be performed and chromosome screening with NGS technology, at the same time, the blastocysts will be frozen, then the blastocysts with normal chromosome will be thawed and transferred.
control group
NO INTERVENTIONAfter blastocyst culture, blastocysts will be transferred
Interventions
Eligibility Criteria
You may qualify if:
- Premenopausal females, age ≥37 years ≤44 years
- Have given birth to a healthy baby
- Bilateral ovaries
- Antral follicle count(AFC)≥10,and Anti Mullerian Hormone (AMH)≥2.0 ng/ml
You may not qualify if:
- Endometriosis disease
- Intrauterine adhesions history; intrauterine membrane polyp, tuberculosis and inflammation,
- Uterine malformation, multiple uterine myoma, uterine intramural myoma \>3cm, submucous myoma;
- Unprocessed hydrosalpinx
- Adverse reproductive history; greater than or equal to 2 times history of unexplained abortion
- Chromosomal abnormalities or other genetic disease
- Infertility caused by male factors, such as puncture testicular, SRT did not see the class A and class B sperm
- Without high quality embryos in past controlled ovarian hyperstimulation (COH)cycles.
- Patients with poor ovarian response, the standard of poor ovarian response accords with Bolognacriteria standard, that is at least meet 2 among the following 3:
- Elder years (≥40 years) or have other known inherited or acquired risk factors that may reduce follicle.
- History of cancellation of the cycles because of less than 3 follicular development, or history of egg number less than 4 after at least using Follicle-Stimulating Hormone(FSH) 150IU once a day.
- Ovarian reserve function test abnormalities, including sinus follicle number less than 5-7 AFC or AMH less than 0.5 to 1.1 ng/ml
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Reproductive & Genetic Hospital of CITIC-XIANGYA
Changsha, Hunan, 410000, China
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- SCREENING
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
August 10, 2016
First Posted
August 16, 2016
Study Start
September 23, 2016
Primary Completion
May 1, 2018
Study Completion
August 1, 2019
Last Updated
January 26, 2022
Record last verified: 2020-03