High Quality Evidence of Chinese Lupus Nephritis (HELP)

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age14+
SponsorSun Yat-sen University

About this trial

The investigators are registering LN patients at recruited hospitals and developing a LN database in China. Patients will be follow-up every year, and both baseline and follow-up information will be entered into the registration system.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Patients who diagnosis as lupus nephritis

Disqualifiers

No

Trial population

Lupus nephritis patients

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

  • No Intervention

    Other intervention

    Registration of all LN patients in the First Affiliated Hospital of Sun Yat-sen University and other hospitals which have signed the contract in China.

Treatment groups

5,000 Participants
are divided into 1 treatment group
Group A: LN patients1 intervention

Trial outcomes

Primary outcomes

1

All-cause mortality and cardiovascular mortality of LN patients

Time frame
10years
2

A composite renal outcome of LN patients

The composite renal outcome defined as doubling of serum creatinine and ESRD (defined as initiation of dialysis or kidney transplantation).

Time frame
10years

Secondary outcomes

Other outcomes

Sponsors and contacts

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