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Clinical Trial Details — Status: Enrolling by invitation

Administrative data

NCT number NCT03805165
Other study ID # Guangdong WCH
Secondary ID
Status Enrolling by invitation
Phase
First received
Last updated
Start date February 1, 2019
Est. completion date December 31, 2019

Study information

Verified date January 2019
Source Guangdong Women and Children Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Make a neonatal jaundiced nomogram on Chinese jaundice data by joinning the major neonate centers all around China.


Description:

Jaundice in common amount Chinese newborn population. The neonatal jaundice guildline was made base on the AAP. guideline. Chinese newborn have their jaundice follow up and treatment plans make base on American neonatel jaundice data. Our group are now planning to have our own neonatel jaundice data by joinning the major neonate centers all around China. A neonatal jaundiced nomogram would be made base on Chinese neonatel jaundice data.


Recruitment information / eligibility

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

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
China Jie Yang Guangzhou Guangdong

Sponsors (1)

Lead Sponsor Collaborator
Guangdong Women and Children Hospital

Country where clinical trial is conducted

China, 

Outcome

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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