Viewing Study NCT00004305



Ignite Creation Date: 2024-05-05 @ 11:22 AM
Last Modification Date: 2024-10-26 @ 9:04 AM
Study NCT ID: NCT00004305
Status: COMPLETED
Last Update Posted: 2005-06-24
First Post: 1999-10-18

Brief Title: Study of Genetic Anomalies of Complement Related Proteins in Patients With IgA Glomerulonephritis
Sponsor: National Center for Research Resources NCRR
Organization: National Center for Research Resources NCRR

Study Overview

Official Title: None
Status: COMPLETED
Status Verified Date: 2002-04
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
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
Detailed Description: 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

Study Oversight

Has Oversight DMC:
Is a FDA Regulated Drug?:
Is a FDA Regulated Device?:
Is an Unapproved Device?:
Is a PPSD?:
Is a US Export?:
Is an FDA AA801 Violation?:
Secondary IDs
Secondary ID Type Domain Link
OSU-94H0338 None None None