Precision diagnosis and treatment of jaundice based on genomics

Status

Recruiting

Phases

Early Phase 1

Study type

Observational

Source

ChiCTR

Registry ID

ChiCTR2100045641

Enrollment

Unknown

Registered

2021-04-20

Start date

2021-05-01

Completion date

Unknown

Last updated

2021-12-06

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

Conditions

jaundice

Interventions

jaundice group:Nil

Eligibility

Sex/Gender

All

Age

No minimum to 0.5 Years

Inclusion criteria

Inclusion criteria: 1. Pathological jaundice. 2. Aged < 6 months, normal birth weight.

Exclusion criteria

Exclusion criteria: 1. Birth history of asphyxia. 2. Jaundice caused by infection, hemolytic, immunopathy and parenteral nutrition. 3. Complicated with multiple organ dysfunction, hematopathy, malignant tumor, heart failure and renal dysfunction and other serious diseases.

Design outcomes

Primary

Measure	Time frame
whole exome sequencing;	—

Secondary

Measure	Time frame
gut microbiota;feacal bile acid;hematuria tandem mass spectrometry;biochemistry analysis;	—

Countries

China

Contacts

Public ContactYe Hong

Fujian Provincial Maternity and Children's Hospital

58646812@qq.com+86 13959186603

Outcome results

None listed

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