- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01628744
Autoantibodies Against Specific Cytokines in Adults With Severe Mycobacterial Infection
June 26, 2012 updated by: China Medical University Hospital
In adult, the prevalence of mycobacterial infections is increased with age is largely unknown.
IFN-gamma-IL-12/23 axis or NF-kappaB pathways might also plays crucial roles in adult against mycobacteria.
Based on this hypothesis, the investigators had applied a functional assay to these pathways in patients with mycobacterial infection.
Study Overview
Status
Unknown
Conditions
Study Type
Observational
Enrollment (Anticipated)
100
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Cheng-?Lung KU, Ph.D
- Phone Number: 3496 (886) (0)3 211-8800
- Email: clku@mail.cgu.edu.tw
Study Locations
-
-
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Taichung, Taiwan
- Recruiting
- Graduate Institute of Clinical Medical Science, China Medical University
-
Principal Investigator:
- Chih Y. Chi, M.D,
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Pateitns with Mycobacterium, Particular to the non Tuberculosis mycobacterium infection, in Taiwan
Description
Inclusion Criteria:
- Patients with mycobacterial infection
Exclusion Criteria:
- Malignancy
- Severe autoimmune
- HIV infection
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
---|
Patients with mycobacterial infection
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Cheng-Lung KU, Ph.D, Graduate Institute of clinical Medical Science, China Medical Univerity, Taiwan
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
January 1, 2011
Study Completion (Anticipated)
December 1, 2014
Study Registration Dates
First Submitted
June 24, 2012
First Submitted That Met QC Criteria
June 26, 2012
First Posted (Estimate)
June 27, 2012
Study Record Updates
Last Update Posted (Estimate)
June 27, 2012
Last Update Submitted That Met QC Criteria
June 26, 2012
Last Verified
June 1, 2012
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- DMR-99-IRB-075-1
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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