Study of Genetic Anomalies of Complement Related Proteins in Patients With IgA Glomerulonephritis
2 other identifiers
observational
105
1 country
1
Brief Summary
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for all trials
1 active site
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Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
January 1, 1998
CompletedFirst Submitted
Initial submission to the registry
October 18, 1999
CompletedFirst Posted
Study publicly available on registry
October 19, 1999
CompletedJune 24, 2005
April 1, 2002
October 18, 1999
June 23, 2005
Conditions
Keywords
Eligibility Criteria
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Sponsors & Collaborators
Study Sites (1)
Ohio State University
Columbus, Ohio, United States
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- STUDY CHAIR
Lee A. Hebert
Ohio State University
Study Design
- Study Type
- observational
- Sponsor Type
- NIH
Study Record Dates
First Submitted
October 18, 1999
First Posted
October 19, 1999
Study Start
January 1, 1998
Last Updated
June 24, 2005
Record last verified: 2002-04