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| Sponsors and Collaborators: |
National Center for Research Resources (NCRR) National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) Ohio State University |
| Information provided by: | National Center for Research Resources (NCRR) |
| ClinicalTrials.gov Identifier: | NCT00004305 |
Purpose
OBJECTIVES: I. Determine whether allelic differences associated with the fourth component of complement, type-1 complement receptor expressed on erythrocytes, and Fc receptor FcgRIII contribute to the pathogenesis of IgA glomerulonephritis (IgA-N).
II. Compare genetic anomalies of these key components in immune complex processing and clearance between juvenile vs adult onset IgA-N vs normal controls.
| Condition |
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IGA Glomerulonephritis |
| Study Type: | Observational |
| Study Design: | Screening |
| Estimated Enrollment: | 105 |
| Study Start Date: | January 1998 |
PROTOCOL OUTLINE:
Participants undergo qualitative genetic analysis of complement-related proteins. Studies include: genomic re-arrangement of 4-gene unit, C4 DNA sequence and RNA expression, type-1 complement receptor DNA sequence, Fc-gamma receptor IIIA isoform analysis, classical and alternative complement activation pathway assays, plasma C4 and C4d protein levels, and immunoglobulin patterns in glomerular deposits.
Eligibility
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Contacts and Locations| United States, Ohio | |||||
| Ohio State University | |||||
| Columbus, Ohio, United States | |||||
| National Center for Research Resources (NCRR) |
| National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) |
| Ohio State University |
| Study Chair: | Lee A. Hebert | Ohio State University |
More Information
| Study ID Numbers: | 199/11791, OSU-94H0338 |
| First Received: | October 18, 1999 |
| Last Updated: | June 23, 2005 |
| ClinicalTrials.gov Identifier: | NCT00004305 |
| Health Authority: | United States: Federal Government |
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