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UnknownNCT02231996

Chronic Granulomatous Disease Study in China

Status
Unknown
Phase
Study type
Observational
Enrollment
50 (estimated)
Sponsor
Shanghai Children's Medical Center · Academic / Other
Sex
All
Age
1 Day – 18 Years
Healthy volunteers
Not accepted

Summary

CGD is a rare inherited primary immunodeficiency which is caused by the defect in one of the subunits of NADPH oxidase complex.We tend to collect and analyze Chinese CGD patients who are diagnosed in hospitals affiliated to Shanghai Jiao Tong University School of Medicine, including clinical feature, laboratory data and genetic information. we aim to find out clinical, distribution, genetic characteristic of CGD in Chinese population, etc., thus further improving the level of diagnosis and treatment for CGD.

Conditions

Timeline

Start date
2014-09-01
Primary completion
2016-08-01
First posted
2014-09-04
Last updated
2014-09-05

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT02231996. Inclusion in this directory is not an endorsement.

Chronic Granulomatous Disease Study in China (NCT02231996) · Clinical Trials Directory