NCT02969174

Brief Summary

To establish a genotyping and extraction technology of non invasive prenatal diagnosis for fetal blood group genotype from cell-free fetal DNA in peripheral blood of pregnant women. To achieve prenatal accurate identification of fetal blood group genotypes,and provide credible theoretical evidence for the prenatal diagnosis and treatment of hemolytic disease of newborn (HDN).

Trial Health

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

November 3, 2016

Completed
18 days until next milestone

First Posted

Study publicly available on registry

November 21, 2016

Completed
Last Updated

November 21, 2016

Status Verified

November 1, 2016

First QC Date

November 3, 2016

Last Update Submit

November 17, 2016

Conditions

Interventions

chengzhong Liu

Eligibility Criteria

Age12 Weeks - 38 Weeks
Sexall
Age GroupsChild (0-17)

You may qualify if:

  • blood samples of pregnant couples,gender/nation/region is unlimited.

You may not qualify if:

  • adipose or hemolytic samples,overdue samples,unidentified samples

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Design

Study Type
expanded access
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
The President of Shanghai Tongji Hospital

Study Record Dates

First Submitted

November 3, 2016

First Posted

November 21, 2016

Last Updated

November 21, 2016

Record last verified: 2016-11