Chronic Granulomatous Disease Study in China

NCT ID: NCT02231996

Last Updated: 2014-09-05

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Total Enrollment

50 participants

Study Classification

OBSERVATIONAL

Study Start Date

2014-09-30

Brief Summary

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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.

Detailed Description

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Conditions

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Granulomatous Disease, Chronic

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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gene mutation

No interventions assigned to this group

Eligibility Criteria

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Inclusion Criteria

* x-linked and AR-linked Chronic Granulomatous Disease
* history of life-threatening severe infections
* A functional assay demonstrating abnormal NADPH oxidase function or clinical history consistent with CGD

Exclusion Criteria

* Presence of other primary immunodeficiency syndromes that do not meet the clinical and laboratory criteria for CGD.
Minimum Eligible Age

1 Day

Maximum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Shanghai Children's Medical Center

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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Shanghai children's medical center

Shanghai, Shanghai Municipality, China

Site Status

Countries

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China

Central Contacts

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jing wu

Role: CONTACT

Other Identifiers

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CGD-20140829

Identifier Type: -

Identifier Source: org_study_id

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