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Recruiting NCT06682507

High Quality Evidence of Guangzhou Lupus Nephritis Cohort (HOPE Cohort)

— Observational Lupus Nephritis (LN)

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An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: No Intervention: Observational Cohort.
Who it may be relevant to
Registry conditions: Lupus Nephritis (LN). Basic parameters: from 14 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
China
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

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Overview

The goal of this observational study is to learn about the long-term renal and patient's survival of lupus nephritis (LN) patients in China. The main question it aims to answer is: Does the renal and patient's survival improved in the long term period? Participants who had renal biopsy proven lupus nephritis in one hospital will be followed up.

Detailed description

Patients from 1996-2016 were retrospective enrolled and patients starting from 2017 were prespective enrolled

Interventions

  • Other No Intervention: Observational Cohort
    No Intervention: Observational Cohort

Primary outcome measures

  • Rate of patients with end stage renal disease [Time frame: From data of enrollment until the data of first documented end stage renal disease, assessed up to 50 years]
Secondary outcome measures (1)
  • Rate of patient's mortality [Time frame: From data of enrollment until the data of death, assessed up to 50 years]

Eligibility criteria

Inclusion criteria

Patients who had biopsy proven lupus nephritis in The First Affiliated Hospital of Sun Yat-sen University

Exclusion criteria

  • less than 14 years old
  • refused to give written consent

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Cohort

Study locations

China · 1 center
  • The First Affiliated Hospital of Sun Yat-sen University — Guangzhou

Identifiers

NCT: NCT06682507 · FirstSunYetSen2016-215

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗