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Study for the clinical phenotype and genotype of primary immunodeficiency disease

Study for the relationship between clinical phenotype and genotype of primary immunodeficiency disease

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2000029463
Enrollment
Unknown
Registered
2020-02-02
Start date
2020-02-01
Completion date
Unknown
Last updated
2020-02-03

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

Conditions

primary immunodeficiency disease

Interventions

patients with suspected primary immunodeficiency:Nil

Sponsors

Children's Hospital of Chongqing Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
No minimum to 18 Years

Inclusion criteria

Inclusion criteria: The Childrens Hospital of Chongqing Medical University and other participating units received and informed the patient, signed the informed consent and agreed to send the patient to the panel of genetic testing related to primary immune deficiency.

Exclusion criteria

Exclusion criteria: (1) Patients with acquired immunodeficiency due to severe infection, malignant tumor, use of immunosuppressants or other causes; (2) There are suspected cases, but the clinical data, including physical examination, blood biochemical examination, imaging examination and other relevant examinations, do not exclude patients with acquired immunodeficiency disease; (3) After receiving the informed notification, the patients with suspected immunodeficiency and their families were explicitly refused to participate in the program.

Design outcomes

Primary

MeasureTime frame
causative genes of primary immunodeficiency disease;—

Countries

China

Contacts

Public ContactZhao Xiaodong

Children's Hospital of Chongqing Medical University

zhaoxd530@aliyun.com+86 023-63620602

Outcome results

None listed

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