Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT04449991

Per-protocol Repeat Kidney Biopsy in Incident Cases of Lupus Nephritis

Led by Karolinska Institutet · Updated on 2025-09-02

206

Participants Needed

1

Research Sites

360 weeks

Total Duration

On this page

Sponsors

K

Karolinska Institutet

Lead Sponsor

U

Université Catholique de Louvain

Collaborating Sponsor

AI-Summary

What this Trial Is About

Lupus nephritis (LN) is one of the most severe complications of systemic lupus erythematosus (SLE). Among people living with SLE, 35-60% will develop LN during the course of the disease. This complication is one of the factors that contribute to deterioration of the renal function. Some centres perform kidney biopsies after completion of treatment for an episode of LN as a part of the treatment evaluation. The term "repeat biopsy" is often used to describe these biopsies. Several studies have reported that repeat kidney biopsies show activity at the level of tissue, even in patients with normal routine blood and urine markers. The investigators strongly believe that this information is important, and should be taken into consideration during decision of treatment. To provide evidence for this, the investigators have designed a collaborative project within the frame of the Lupus Nephritis Trials Network. With this research project, the investigators want to contribute to an increased proportion of patients with LN who achieve remission (inactivity) of LN, and a reduced proportion of patients who worsen in renal function in the long term. Patients with SLE who develop a first episode of LN will be asked to participate in this project, and will receive treatment according to current guidelines. Half of the patients will undergo a repeat biopsy 12 months later, and half of the patients will not. The selection of patients who will undergo or not undergo repeat biopsy will be random. Patients with high disease activity at the level of kidney tissue will receive more intense immunosuppressive treatment. Patients who have not undergone repeat biopsy will continue to be treated according to standard routine. The investigators will compare the results of treatment between the group of patients who underwent and the group of patients who did not undergo repeat biopsy, with regard to (i) complete disease inactivity at month 24 and (ii) renal function at month 60 from treatment initiation. The investigators expect that significantly greater proportions of patients in the repeat biopsy group will have inactive disease at month 24 and adequate levels of renal function at month 60. This will provide support for performing repeat biopsies as a part of the treatment evaluation, in order to optimise the therapeutic management and improve the long-term prognosis of patients with LN.

CONDITIONS

Official Title

Per-protocol Repeat Kidney Biopsy in Incident Cases of Lupus Nephritis

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Meet the EULAR/ACR classification criteria for systemic lupus erythematosus (SLE)
  • 18 years of age or older
  • New diagnosis of biopsy-proven proliferative or membranous lupus nephritis with urine protein-to-creatinine ratio of 1 g/g or higher
  • Agree to the possibility of repeat kidney biopsy at 12 months after baseline
  • Starting treatment with intravenous methylprednisolone pulses, oral prednisone 0.3-0.5 mg/kg/day with tapering, hydroxychloroquine (unless contraindicated), ACE inhibitors or ARBs, and either mycophenolate mofetil (2-3 g/day) or intravenous cyclophosphamide per Euro-Lupus regimen
  • Optional add-on therapies such as calcineurin inhibitors or biologics
Not Eligible

You will not qualify if you...

  • Antiphospholipid syndrome nephropathy
  • Pregnancy at the start of the study
  • Medical reasons preventing kidney biopsy, including low platelets below 50,000/µL, uncontrolled high blood pressure, or end-stage kidney disease
  • Expected poor adherence to therapy
  • Medical conditions that interfere with evaluating outcomes
  • Unable to read or sign the informed consent form

AI-Screening

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Trial Site Locations

Total: 1 location

1

Karolinska University Hospital

Stockholm, Sweden, 17676

Actively Recruiting

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Research Team

I

Ioannis Parodis, MD PhD | Associate Professor

CONTACT

F

Farah Tamirou, MD PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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