Jaundice, Neonatal Clinical Trial
Official title:
Hour-specific Transcutaneous Bilirubin in Healthy Term and Near-term Newborns of China
Verified date | January 2019 |
Source | Guangdong Women and Children Hospital |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
Make a neonatal jaundiced nomogram on Chinese jaundice data by joinning the major neonate centers all around China.
Status | Enrolling by invitation |
Enrollment | 3000 |
Est. completion date | December 31, 2019 |
Est. primary completion date | March 31, 2019 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | N/A to 7 Days |
Eligibility |
Inclusion Criteria: gestational age more than 35 weeks(=35) - Exclusion Criteria: all kinds of congenital diseases, infants with pathologic jaundice |
Country | Name | City | State |
---|---|---|---|
China | Jie Yang | Guangzhou | Guangdong |
Lead Sponsor | Collaborator |
---|---|
Guangdong Women and Children Hospital |
China,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Hour-specific Transcutaneous Bilirubin Level | make neonatal jaundiced nomogram base on the hour-specific transcutaneous bilirubin data | 1 year |
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