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Preimplantation genetic diagnosis using single-nucleotide polynorphism(SNP) improve the in vitro ferilization outcomes for translocation carriers: a perspective followed cohort study

Preimplantation genetic diagnosis using single-nucleotide polynorphism(SNP) improve the in vitro ferilization outcomes for translocation carriers: a perspective one arm followed cohort study

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-PRCH-14004239
Enrollment
Unknown
Registered
2014-01-15
Start date
2014-04-01
Completion date
Unknown
Last updated
2017-04-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

in vitro fertilization attampted translocation carriers patients

Interventions

using snp group:Preimplantation genetic diagnosis using single-nucleotide polynorphism
control group:snp cancelled or refused

Sponsors

Chongqing Obstetrics and Gynaecology Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
26 Years to 34 Years

Inclusion criteria

Inclusion criteria: translocation carriers patients who attampted in vitro fertilization

Exclusion criteria

Exclusion criteria: chromosome disorder patients except translocation carriers

Design outcomes

Primary

MeasureTime frame
live birth rate;—

Contacts

Public ContactHuang Guoning

Chongqing Obstetrics and Gynaecology Hospital

gnhuang217@sina.com+86 13808335727

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026