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Evaluating of the distribution of glucose-6-phosphate dehydrogenase deficiency (G6PD) and gene mutations in Chinese newborns

Evaluating of the distribution of glucose-6-phosphate dehydrogenase deficiency (G6PD) and gene mutations in Chinese newborns

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-SOC-17014057
Enrollment
Unknown
Registered
2017-12-20
Start date
2014-01-01
Completion date
Unknown
Last updated
2018-01-29

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

Conditions

glucose-6-phosphate dehydrogenase deficiency

Interventions

Newborns went throug basic screening:Testing of the Glucose-6 phosphate dehydrogenase activity
Newborns suspected with G6PD deficiency:Gene diagnosis
Female newborns with normal Glucose-6 phosphate dehydrogenase activity:Gene diagnosis
Male newborns with normal glucose-6 phosphate dehydrogenase activity:Gene diagnosis

Sponsors

Center for Clinical Molecular Medicine & Newborn Screening Center, Children’s Hospital of Chongqing Medical University, Chongqing, China
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Neonatal screening: full-term, three days after birth, full breast-feeding after birth. 2. Selected from continuous screening time, can not be intermittent selected, can not be artificially selected.

Exclusion criteria

Exclusion criteria: 1. Samples with incomplete clinical information

Design outcomes

Primary

MeasureTime frame
Activity of the glucose-6-phosphate dehydrogenase;G6PD gene;—

Countries

China

Contacts

Public ContactLin Zhou

Center for Clinical Molecular Medicine & Newborn Screening Center, Children’s Hospital of Chongqing Medical University, Chongqing, China

zoulin74@126.com+86 18623121280

Outcome results

None listed

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