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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01538433
Other study ID # GGH201107
Secondary ID
Status Completed
Phase N/A
First received February 19, 2012
Last updated August 17, 2015
Start date February 2012
Est. completion date December 2012

Study information

Verified date August 2013
Source Guangdong General Hospital
Contact n/a
Is FDA regulated No
Health authority China: Ethics Committee
Study type Observational

Clinical Trial Summary

This is a survey of factors which affect a pathologically defined early or delayed diagnosis of IgA nephropathy in Guangdong General Hospital, Guangzhou, China. An early or delayed diagnosis of IgA nephropathy is pathologically defined using the recently published Oxford classification of IgA nephropathy. The factors to be surveyed include health examination including urine test, socioeconomic status of patients including education,etc.


Recruitment information / eligibility

Status Completed
Enrollment 603
Est. completion date December 2012
Est. primary completion date December 2012
Accepts healthy volunteers No
Gender Both
Age group 14 Years to 80 Years
Eligibility Inclusion Criteria:

- biopsy-proven IgA Nephropathy patients in Guangdong General Hospital, Guangzhou,China

Study Design

Time Perspective: Retrospective


Related Conditions & MeSH terms


Locations

Country Name City State
China Nephrology Department,Guangdong General Hospital Guangzhou Guangdong

Sponsors (1)

Lead Sponsor Collaborator
Guangdong General Hospital

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Factors potentially affecting an early or delayed diagnosis of IgA Nephropathy Before the biopsy No
Secondary Glomerular filtration rate(GFR) decline rate or reaching end-stage renal disease (ESRD) or doubling of serum creatinine after the biopsy No
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