The Chinese Registry of Prognostic Study of IgA Nephropathy (CRPIGA)

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
AgeNot listed
SponsorRuijin Hospital

About this trial

1. Establish an IgAN cohort collaboration group and expert committee to carry out registration research. 2. Construct IgAN structured data set standards, formulate structured data collection templates of diagnosis and treatment , and establish multi-center data integration systems on this basis. 3. Establish a standardized IgAN database for combined Hospital Information System and the big data platform of the Medical Federation. 4. Develop IgAN database managements and open standards for data sharing, and carry out high-quality clinical or basic research.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

No age limit, no gender limit;

Kidney biopsy confirmed primary IgA nephropathy;

Sign the informed consent form voluntarily

Disqualifiers

IgA nephropathy is secondary to systemic diseases such as systemic lupus erythematosus and allergic purpura;

IgAN is clinically diagnosed but not confirmed by pathology;

The patient refuses to participate;

Patients judged by other investigators to be unsuitable for inclusion in the study.

Trial population

Biopsy-proven primary IgAN patients

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

Not listed

Trial groups

No trial groups listed

Trial outcomes

Primary outcomes

1

The proportion of a decline in estimated glomerular filtration rate by > 50% from baseline

To evaluate the renal function

Time frame
1 year
2

The proportion of doubling serum creatinine compared with baseline

To evaluate the renal function

Time frame
1 year
3

Incidence of ESRD

To evaluate the renal function

Time frame
1 year

Secondary outcomes

1

Incidence of cardiovascular events

Record of Cardiovascular events during follow-up period

Time frame
1 year
2

Incidence of All-cause death

Record of All-cause death during follow-up period

Time frame
1 year

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Ruijin Hospital

Lead sponsor

RenJi Hospital

Collaborator

Huashan Hospital

Collaborator

Shanghai Ninth People's Hospital Affiliated to Shanghai Jiao Tong University

Collaborator