Systemic Lupus Erythematosus NephritisNCT06642402
Monitoring Lupus Nephritis Through Urinary Extracellular Vesicles
An observational study of Systemic Lupus Erythematosus Nephritis, run by Kolding Sygehus at 4 sites in Denmark.
Trial summary
Lupus nephritis (LN) is a severe manifestation of systemic lupus erythematosus (SLE) that can lead to irreversible kidney damage if not detected and managed promptly. LN is classified and treated based on its histopathological features obtained by invasive kidney biopsy. Read more about this study
- Who is it for?
- Ages 18 years and olderHealthy volunteers can take part
- Conditions the study is for
- Systemic Lupus Erythematosus Nephritis
- What is being tested?
- Kidney biopsy, Urinary extracellular vesicle testing and Autoimmunity in plasma
- How many people
- 40 participants
- Where
- 4 sitesDenmark
- Study dates
- 15 Nov 2024to 1 May 2030
- How long will I take part?
- 1 Year
- Phase
- Observational
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- Healthy volunteers accepted
- Adult, Older adult
Study population: Patients known with SLE with and without kidney involvement, a biopsy control and a group of healthy controls.
Who may be able to join
- > 18 years old
- Fulfilling the 2019 EULAR/ACR classification criteria
- Positive autoantibodies, medical history and obejctive examination compatible with SLE
- Referred to kidney biopsy
- > 18 years old
- Fulfilling the 2019 EULAR/ACR classification criteria
Show all 14Show fewer
- Positive autoantibodies, medical history and obejctive examination compatible with SLE
- Normal plasma creatinine
- Urine albumine/creatinine < 100 mg/g
- > 18 years old
- No known kidney disease
- > 18 years old
- Negative autoantibiodies and immunoglobulines
- Referred to kidney biopsy
Who cannot join
- Lack of ability or willingness to provide informed consent
- Significant comorbidity, which is considered to potentially impact the outcome
- SLE patients with no sign of kidney disease
- Lack of ability or willingness to provide informed consent
- Significant comorbidity, which is considered to potentially impact the outcome
- Healthy controls:
Show all 13Show fewer
- Lack of ability or willingness to provide informed consent
- Urine albumin-creatinine ratio > 100 mg/g or proteinuria > 100 mg/day
- Postive autoantibodies
- Significant comorbidity, which is considered to potentially impact the outcome
- Biopsy control:
- Lack of ability or willingness to provide informed consent
- Significant comorbidity, which is considered to potentially impact the outcome
Trial locations and contacts
4 sites in 1 country. Contact the study team or a site near you to ask about taking part.
Anne D Thuesen, MD, phd, clinical lector contact
Denmark4 sites, 4 recruiting
- Not yet recruiting
Kolding Hospital
Kolding
Anne D Thuesen, Head of research, MD, phd, 004576360555, anne.daugaard.thuesen2@rsyd.dk
- Not yet recruiting
Department of Nephrology
Odense, 5000
michael Aarup, MD, consultant
- Recruiting
Department of Rheumatology
Odense, 5000
Henrik Z Langkilde, MD, 21279653, henrik.zachar.langkilde@rsyd.dk
- Not yet recruiting
Univesity of Southern Denmark
Odense, 5230
Per Svenningsen, professor, 004565501000, psvenningsen@health.sdu.dk
About this study
Official title: Monitoring and Detecting Lupus Nephritis Through Urinary Extracellular Vesicles in Urine
Lupus nephritis (LN) is a severe manifestation of systemic lupus erythematosus (SLE) that can lead to irreversible kidney damage if not detected and managed promptly. LN is classified and treated based on its histopathological features obtained by invasive kidney biopsy. Recent research has suggested urinary extracellular vesicles (uEVs) as potential non-invasive biomarkers. The primary objective of this prospective study is to investigate the utility of uEVs in LN.
Read the detailed description
Introduction: Lupus nephritis (LN) is a severe manifestation of systemic lupus erythematosus (SLE) that can lead to irreversible kidney damage if not detected and managed promptly. LN is classified based on its histopathological features. The classification helps in determining the severity and appropriate treatment strategies for the condition and to rule out other conditions that may mimic the clinical picture of LN. The classification system most commonly used is the International Society of Nephrology/Renal Pathology Society (ISN/RPS) classification, which divides lupus nephritis into six classes: I) Minimal Change, II) Mesangial Proliferative LN, III) Focal Proliferative LN, IV) Diffus proliferative LN, V) Membranous LN, VI) Advanced Sclerosing LN. The classification requires invasive kidney biopsies, which are hardly accessible and associated with potential complications and patient discomfort. Furthermore the kidney biopsy only represent a small part of the kidney. Recent research has suggested urinary extracellular vesicles (uEVs) as potential non-invasive biomarkers for kidney diseases, including LN. uEVS are small nano-sized extracellular vesicles of endosomal origin, which are secreted into the urine through fusion of multivesicular bodies with the plasma membrane. Thus, they could represent a promising liquid biopsy that reflects the pattern and/or severity of renal injury.
Hypothesis: The primary objective of this prospective study is to investigate the utility of urinary exosomes as non-invasive biomarkers for monitoring the activity and progression of lupus nephritis.
Methods: SLE patients, fulfilling the 2019 EULAR/ACR classification criteria, referred to kidney biopsy, will be recruited from Department of Rheumatology and Department of Nephrology at Odense University Hospital. Detailed demographic and clinical data including age, sex, ethnicity, medicine, duration of SLE activity, SLE damage and laboratory results will be collected from each patient. Activity of SLE at the time of biopsy will be evaluated using SLE disease activity index 2000 (SLEDAI-2K). SLE damage will be evaluated in accordance with the SLICC damage index. Spot-urine samples will be collected, added protease-inhibitors and frozen at -80 degree. UEVs will be isolated using polyethylene glycol (PEG) precipitation, the concentration of uEV will be determined and protein accessed using western blotting and/or PCR. Glomerular specific uEVs will be isolated and previous developed tests will be applied to detect the membrane attack complex (MAC)/C5b-9 complex. uEVs from plasma/serum will be isolated to test for correlation with uEVs. Kidney biopsies will be histological analyzed at Department of Pathology by experienced nephropathologists according to existing clinical guidelines. Differences in uEV cargo between SLE patients with and without lupus nephritis will be analyzed using appropriate statistical tests. Correlations between uEV biomarkers, histological differences on the kidney biopsy and disease activity will be evaluated using Pearson's correlation analysis.
Perspective: This prospective study aims to establish urinary extracellular vesicles as potential non-invasive biomarkers for monitoring lupus nephritis in SLE patients. The findings from this research may lead to the development of more efficient and patient-friendly approaches for LN management, enabling timely interventions and improved renal outcomes in SLE patients.
- Conditions
- Systemic Lupus Erythematosus Nephritis
- Being tested
- Kidney biopsy, Urinary extracellular vesicle testing, Autoimmunity in plasma
- Keywords
- Systemic Lupus Erythoematosus nephritis, Lupus nephritis, complement activation, kidney biopsy
- Medical subject headings
- Lupus Nephritis
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Kidney biopsyDiagnostic test
Also called No expected complement activation
Patient refered to kidney biopsy independent of the presented study
Urinary extracellular vesicle testingDiagnostic test
Urinary extracellular vesicles will be isolated and tested for complement activation and other markers of kidney disease
Autoimmunity in plasmaDiagnostic test
Expected autoimmunity in plasma isolated from blood samples
| Study group | Role | What they receive |
|---|---|---|
| Systemic lupus erythomatosus with lupus nephritis | SLE patients with kidney involvement Receives: Diagnostic Test: Kidney biopsy; Diagnostic Test: Urinary extracellular vesicle testing; Diagnostic Test: Autoimmunity in plasma | |
| Systemic lupus erythomatosus without lupus nephritis | SLE patients, fulfilling the 2019 EULAR/ACR classification criteria with no sign of kidney disease Receives: Diagnostic Test: Urinary extracellular vesicle testing; Diagnostic Test: Autoimmunity in plasma | |
| Healthy controls | Healthy controls Receives: Diagnostic Test: Urinary extracellular vesicle testing | |
| Biopsy controls | A biopsy control group with no predictive complement activation referred to biopsy Receives: Diagnostic Test: Kidney biopsy; Diagnostic Test: Urinary extracellular vesicle testing |
What is being measured
The primary outcome is the main question the study is designed to answer.
Correlation between kidney biopsy and urinay extracellular vesicles
The primary outcome is to investigate the correlation between histological findings from kidney biopsy and urinary extracelluar vesicles, with the aim of assessing whether there is concordance between the two methods in relation to disease severity and classification.
Measured: Urinary extracellular vesicles will be isolated from urine collected at the day of kidney biopsy/baseline. Analysis will be performed when all samples are collected. Estimated after 5 years.
Complement activation in urinary extracellular vesicles
Urinary extracellular vesicles will be isolated. Complement activation will be detected using an in-house ELISA assay
Measured: Measured on urinary extracellular vesicles obtained at the day of biopsy/baseline. Analysis will be performed when all samples are collected, estimated after 5 years.
Secondary outcomes (1)
Correlation between urinary extracellular vesicles and extracellular vesicles from plasma
A seconday outcome is to invesigate the correlation between urinary extracellular vesicles and extracellular vesicles from plasma, to see if the same results could be obtained in plasma samples
Measured: Blood- og and urine samples will be collected at the day of kidney biopsy/baseline. Analysis will be performed when all samples are collecting, estimated after 5 years.
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted15 Oct 2024
- Study start15 Nov 2024
- Primary completion1 May 2029 (estimated)
- Study completion1 May 2030 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Systemic Lupus Erythematosus NephritisStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Cohort
- Time perspective
- Prospective
- Enrolment
- 40 participants (estimated)
- Target duration
- 1 Year
Sponsor and investigators
- Lead sponsor
- Kolding Sygehus
- Sponsor type
- University, hospital or other
- Collaborators
- University of Southern Denmark, Odense University Hospital
- Responsible party
- Sponsor
- Investigators
- Anne F Christensen, Chief of Medicine, MD, phd, Study chair, Sygehus Lillebaelt, Kolding Hospitl
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06642402
- Sponsor's protocol ID
- SLELNuEV
- Status last verified
- Sep 2025
- First submitted
- 11 Oct 2024
- Last updated
- 9 Sep 2025
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Undecided
Study at a glance
From the registry record, last updated by the sponsor on 9 Sep 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Monitoring and Detecting Lupus Nephritis Through Urinary Extracellular Vesicles in Urine
- ClinicalTrials.gov ID
- NCT06642402
- Acronym / sponsor ID
- SLELNuEV
- Conditions
- Systemic Lupus Erythematosus Nephritis
- Keywords
- Systemic Lupus Erythoematosus nephritis, Lupus nephritis, complement activation, kidney biopsy
- Study type
- Observational
- Recruitment status
- Recruiting
- Enrolment
- 40 participants (estimated)
- Lead sponsor
- Kolding SygehusUniversity, hospital or other
- Collaborators
- University of Southern Denmark, Odense University Hospital
- Study start
- 15 Nov 2024 (actual)
- Primary completion
- 1 May 2029 (estimated)
- Study completion
- 1 May 2030 (estimated)
- First posted
- 15 Oct 2024 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
Lupus nephritis (LN) is a severe manifestation of systemic lupus erythematosus (SLE) that can lead to irreversible kidney damage if not detected and managed promptly. LN is classified and treated based on its histopathological features obtained by invasive kidney biopsy. Recent research has suggested urinary extracellular vesicles (uEVs) as potential non-invasive biomarkers. The primary objective of this prospective study is to investigate the utility of uEVs in LN.
Detailed description
Introduction: Lupus nephritis (LN) is a severe manifestation of systemic lupus erythematosus (SLE) that can lead to irreversible kidney damage if not detected and managed promptly. LN is classified based on its histopathological features. The classification helps in determining the severity and appropriate treatment strategies for the condition and to rule out other conditions that may mimic the clinical picture of LN. The classification system most commonly used is the International Society of Nephrology/Renal Pathology Society (ISN/RPS) classification, which divides lupus nephritis into six classes: I) Minimal Change, II) Mesangial Proliferative LN, III) Focal Proliferative LN, IV) Diffus proliferative LN, V) Membranous LN, VI) Advanced Sclerosing LN. The classification requires invasive kidney biopsies, which are hardly accessible and associated with potential complications and patient discomfort. Furthermore the kidney biopsy only represent a small part of the kidney. Recent research has suggested urinary extracellular vesicles (uEVs) as potential non-invasive biomarkers for kidney diseases, including LN. uEVS are small nano-sized extracellular vesicles of endosomal origin, which are secreted into the urine through fusion of multivesicular bodies with the plasma membrane. Thus, they could represent a promising liquid biopsy that reflects the pattern and/or severity of renal injury.
Hypothesis: The primary objective of this prospective study is to investigate the utility of urinary exosomes as non-invasive biomarkers for monitoring the activity and progression of lupus nephritis.
Methods: SLE patients, fulfilling the 2019 EULAR/ACR classification criteria, referred to kidney biopsy, will be recruited from Department of Rheumatology and Department of Nephrology at Odense University Hospital. Detailed demographic and clinical data including age, sex, ethnicity, medicine, duration of SLE activity, SLE damage and laboratory results will be collected from each patient. Activity of SLE at the time of biopsy will be evaluated using SLE disease activity index 2000 (SLEDAI-2K). SLE damage will be evaluated in accordance with the SLICC damage index. Spot-urine samples will be collected, added protease-inhibitors and frozen at -80 degree. UEVs will be isolated using polyethylene glycol (PEG) precipitation, the concentration of uEV will be determined and protein accessed using western blotting and/or PCR. Glomerular specific uEVs will be isolated and previous developed tests will be applied to detect the membrane attack complex (MAC)/C5b-9 complex. uEVs from plasma/serum will be isolated to test for correlation with uEVs. Kidney biopsies will be histological analyzed at Department of Pathology by experienced nephropathologists according to existing clinical guidelines. Differences in uEV cargo between SLE patients with and without lupus nephritis will be analyzed using appropriate statistical tests. Correlations between uEV biomarkers, histological differences on the kidney biopsy and disease activity will be evaluated using Pearson's correlation analysis.
Perspective: This prospective study aims to establish urinary extracellular vesicles as potential non-invasive biomarkers for monitoring lupus nephritis in SLE patients. The findings from this research may lead to the development of more efficient and patient-friendly approaches for LN management, enabling timely interventions and improved renal outcomes in SLE patients.
Study design
- Observational model
- Cohort
- Time perspective
- Prospective
- Target follow-up
- 1 Year
- Number of arms
- 4
| Arm | Type | Receives |
|---|---|---|
| Systemic lupus erythomatosus with lupus nephritis | – | Diagnostic Test: Kidney biopsy, Diagnostic Test: Urinary extracellular vesicle testing, Diagnostic Test: Autoimmunity in plasmaSLE patients with kidney involvement |
| Systemic lupus erythomatosus without lupus nephritis | – | Diagnostic Test: Urinary extracellular vesicle testing, Diagnostic Test: Autoimmunity in plasmaSLE patients, fulfilling the 2019 EULAR/ACR classification criteria with no sign of kidney disease |
| Healthy controls | – | Diagnostic Test: Urinary extracellular vesicle testingHealthy controls |
| Biopsy controls | – | Diagnostic Test: Kidney biopsy, Diagnostic Test: Urinary extracellular vesicle testingA biopsy control group with no predictive complement activation referred to biopsy |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult, Older adult
- Study population
- Patients known with SLE with and without kidney involvement, a biopsy control and a group of healthy controls.
Key inclusion criteria (14 listed)
- > 18 years old
- Fulfilling the 2019 EULAR/ACR classification criteria
- Positive autoantibodies, medical history and obejctive examination compatible with SLE
- Referred to kidney biopsy
- > 18 years old
Key exclusion criteria (13 listed)
- Lack of ability or willingness to provide informed consent
- Significant comorbidity, which is considered to potentially impact the outcome
- SLE patients with no sign of kidney disease
- Lack of ability or willingness to provide informed consent
- Significant comorbidity, which is considered to potentially impact the outcome
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Kidney biopsyAlso: No expected complement activationPatient refered to kidney biopsy independent of the presented study | Diagnostic test | Biopsy controls, Systemic lupus erythomatosus with lupus nephritis |
| Urinary extracellular vesicle testingUrinary extracellular vesicles will be isolated and tested for complement activation and other markers of kidney disease | Diagnostic test | Biopsy controls, Healthy controls, Systemic lupus erythomatosus with lupus nephritis, Systemic lupus erythomatosus without lupus nephritis |
| Autoimmunity in plasmaExpected autoimmunity in plasma isolated from blood samples | Diagnostic test | Systemic lupus erythomatosus with lupus nephritis, Systemic lupus erythomatosus without lupus nephritis |
Primary outcome
Correlation between kidney biopsy and urinay extracellular vesicles
Time frame: Urinary extracellular vesicles will be isolated from urine collected at the day of kidney biopsy/baseline. Analysis will be performed when all samples are collected. Estimated after 5 years.
The primary outcome is to investigate the correlation between histological findings from kidney biopsy and urinary extracelluar vesicles, with the aim of assessing whether there is concordance between the two methods in relation to disease severity and classification.
Complement activation in urinary extracellular vesicles
Time frame: Measured on urinary extracellular vesicles obtained at the day of biopsy/baseline. Analysis will be performed when all samples are collected, estimated after 5 years.
Urinary extracellular vesicles will be isolated. Complement activation will be detected using an in-house ELISA assay
1 secondary outcome
Correlation between urinary extracellular vesicles and extracellular vesicles from plasma
Time frame: Blood- og and urine samples will be collected at the day of kidney biopsy/baseline. Analysis will be performed when all samples are collecting, estimated after 5 years.
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 9 Sep 2025.
- Individual participant dataSharing planned: Undecided
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
Anne D Thuesen, MD, phd, clinical lector contact
Anne F Christensen, Chief of Medicine, MD, phd study chair
Sygehus Lillebaelt, Kolding Hospitl
4 sites in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Systemic Lupus Erythematosus Nephritis, run by Kolding Sygehus at 4 sites in Denmark.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 14 inclusion and 13 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: looking for participants now, as of the sponsor's last update on 9 Sep 2025. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 4 sites in Denmark. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Contact Rikke Z Langkilde, MD, phd (4530281347, rikke.zachar.langkilde@rsyd.dk), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Correlation between kidney biopsy and urinay extracellular vesicles (time frame: Urinary extracellular vesicles will be isolated from urine collected at the day of kidney biopsy/baseline. Analysis will be performed when all samples are collected. Estimated after 5 years.). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 9 Sep 2025.