SARS-CoV 2NCT04378686
Serological Testing for COVID-19 (SARS-CoV-2) in ESKD
An observational study of SARS-CoV 2 and End Stage Renal Failure on Dialysis, run by Universitaire Ziekenhuizen KU Leuven at 3 sites in Belgium.
Trial summary
Starting in late 2019, the world is facing a pandemic with the SARS-CoV-2 virus. Patients with end-stage kidney disease and on treatment with renal replacement therapy are high risk patients, as they are unable to maximize social distancing. Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- SARS-CoV 2, End Stage Renal Failure on Dialysis
- What is being tested?
- dialysis
- How many people
- 500 participants
- Where
- 3 sitesBelgium
- Study dates
- 23 Apr 2020to 12 Dec 2022
- Phase
- Observational
- Are there results?
- None posted in the registry
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
- No healthy volunteers
- Adult, Older adult
Study population: Patients with end-stage kidney disease (ESKD) receiving renal replacement therapy
Who may be able to join
- Patients with end-stage kidney disease (ESKD) receiving renal replacement therapy
- Age 18 years or older
- Treated at University Hospitals Leuven, or Jessa Ziekenhuis Hasselt
- Providing informed consent
Who cannot join
- Refusal to provide informed consent
- Transfer to another dialysis unit
Trial locations and contacts
3 sites in 1 country.
Belgium3 sites
Jessa Ziekenhuis
Hasselt, Limburg, 3500
University Hospitals Leuven
Leuven, 3000
Sint Trudo
Sint-Truiden, Limburg, 3800
About this study
Official title: A Comparative Study of Symptom-driven Surveillance vs. Cross-sectional Serological Screening of SARS-CoV-2 Infection of Patients With End-stage Kidney Disease Receiving Renal Replacement Therapy
Starting in late 2019, the world is facing a pandemic with the SARS-CoV-2 virus. Patients with end-stage kidney disease and on treatment with renal replacement therapy are high risk patients, as they are unable to maximize social distancing.
We plan to gather epidemiological data using two different diagnostic approaches. We will compare a symptom-driven screening, in combination with a nasopharyngeal swab plus computed tomography (clinical approach) against serological surveillance.
Read the detailed description
In late 2019, a cluster of patients with unexplained pneumonia was linked to a novel beta-coronavirus, now known as severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) 1. The world health organization subsequently has coined this disease as COVID-19. By the time the scientific community was alerted, the epidemiological data suggested that the virus had already spread to other regions of mainland China, as well as foreign cities with close transport links to the original epicenter 2. The world initially answered by divergent responses. Two months on, we are experiencing a devastating pandemic with local outbreaks across all continents.
As more and more patients arrive at the hospitals, our focus is drawn to the acute and the important issues, treating large numbers of patients in grave condition. The surge in patients requiring medical care may overwhelm even the most sophisticated healthcare systems 3. The approach adopted by almost all nations is to 'flatten the curve', i.e. to reduce peak demand of healthcare resources 4. While individual countries follow different paths, the common denominator is to maximize social distancing. The main goal is to reduce the basic reproduction number (R0) as much as possible, to ideally less than 1.
An overview of the clinical characteristics of confirmed cases in China alerted the world that young age does not protect against infection 5. Disease severity, however, varies by age with more elderly people becoming seriously ill, and by underlying medical condition(s) 6. The impact on peak medical demand thus will be even greater if we succeed in maximizing social distancing of the most vulnerable and most frail patients, those who are more likely to become seriously ill.
This is, however, difficult for dialysis patients who cannot self-isolate and cannot avoid multiple contacts per week with health care workers and other patients. While isolating dialysis patients and health care workers with a suspected SARS-CoV-2 infection is important to limit transmission of the virus, these measures are insufficient to avoid transmission since it is estimated that asymptomatic or paucisymptomatic people play a major role in the spread of the virus. So far, epidemiological data in patients on IHD during an SARS-CoV-2 outbreak are limited. A single case-series of cases from China has been reported in prepublication. 37 out of 230 patients were infected with SARS-CoV-2, of which 6 died (crude mortality rate 16.2%). The authors suggest that not all of these died directly from the consequences of COVID-19. However, adjudication of cause of death might differ in future case series.
The current gold standard for the diagnosis of acute respiratory syndrome due to SARS-CoV-2 (COVID-19) is the detection of viral RNA in respiratory tract samples. The sensitivity of a negative PCR result is, however, not 100%. False-negatives can occur, especially when using nasopharyngeal swabs (positivity rate estimated at 54%-74%) due to sampling error and in patients with low viral loads, especially in patients who present at day 8 or later and mild cases. While a CT scan can be a valuable tool in patients with a suspicion of COVID-9, measurement of antibodies against SARS-CoV-2 is the only reliable way to estimate the prevalence of SARS-CoV-2 infection since patients can be pauci-symptomatic or asymptomatic.
A number questions remain regarding the use of antibodies for epidemiologic studies and to determine immunity. Can someone have a colonization with SARS-CoV-2 without developing IgG antibodies? In this case, would this person be protected against reinfection? Doctors of the University of Bonn recently reported on April 9th (H. Streeck et al.,data not yet published) that only 15% of a sample of 1.000 inhabitants of the small town Gangelt, a local hotspot in North Rhine Westphalia tested positive for IgG antibodies. These data suggest that even in severely affected regions the critical threshold for herd immunity might not have been reached. This means that there is a significant risk of new outbreaks, particularly after schools might reopen later (maybe in summer 2020, and in fall 2020).
Given that dialysis patients are at the same time potentially more vulnerable to SARS-CoV-2 infection, and cannot self-isolate, it is important to closely monitor this group of patients. A second benefit of this population is that it easily accessible for blood sampling, and close clinical follow-up is ensured.
The aim of this study is to determine the prevalence of patients who were infected with SARS-CoV-2 by measuring IgG antibodies at different time points.
Trial objectives The aim of the current study is to collect epidemiological data of the incidence of severe acute respiratory syndrome Corona Virus type 2 (SARS-CoV-2) infections patients with end-stage kidney disease in a Belgian Hospital setting.
The objective is to compare two means of detection of infection, one symptom-driven surveillance and a second based on cross-sectional serology.
Primary endpoints Positive serology for SARS-CoV-2 at census date(s)
Secondary endpoints Detection of SARS-CoV-2 infection by symptom-driven surveillance
Trial Design Cross-sectional and longitudinal observational study of prevalent patients with end-stage kidney disease
- Conditions
- SARS-CoV 2, End Stage Renal Failure on Dialysis
- Being tested
- dialysis
- Keywords
- nasopharyngeal swab, Chest CT, serology
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
dialysisOther
treatment with dialysis. This can be hemodialysis, hemodiafiltration, peritoneal dialysis
| Study group | Role | What they receive |
|---|---|---|
| ESKD | Patients with ESKD and on treatment with any form of dialysis Receives: Other: dialysis |
What is being measured
The primary outcome is the main question the study is designed to answer.
Antibodies against SARS-CoV-2
serology to test for IgG and IgM antibodies against SARS-CoV-2
Measured: one year
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted7 May 2020
- Study start23 Apr 2020
- Primary completion12 Dec 2022
- Study completion12 Dec 2022
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for SARS-CoV 2Studies of the same condition, open and under way.
- More trials run by Universitaire Ziekenhuizen KU LeuvenThe sponsor's other registered studies.
- 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
- 500 participants (actual)
Sponsor and investigators
- Lead sponsor
- Universitaire Ziekenhuizen KU Leuven
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
- Investigators
- Bjorn Meijers, MD, PhD, Principal investigator, UZ Leuven
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT04378686
- Sponsor's protocol ID
- S64000
- Status last verified
- Jul 2024
- First submitted
- 5 May 2020
- Last updated
- 3 Jul 2024
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Undecided: undecided
Study at a glance
From the registry record, last updated by the sponsor on 3 Jul 2024. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- A Comparative Study of Symptom-driven Surveillance vs. Cross-sectional Serological Screening of SARS-CoV-2 Infection of Patients With End-stage Kidney Disease Receiving Renal Replacement Therapy
- ClinicalTrials.gov ID
- NCT04378686
- Acronym / sponsor ID
- S64000
- Conditions
- SARS-CoV 2, End Stage Renal Failure on Dialysis
- Keywords
- nasopharyngeal swab, Chest CT, serology
- Study type
- Observational
- Recruitment status
- Completed
- Enrolment
- 500 participants (actual)
- Lead sponsor
- Universitaire Ziekenhuizen KU LeuvenUniversity, hospital or other
- Study start
- 23 Apr 2020 (actual)
- Primary completion
- 12 Dec 2022 (actual)
- Study completion
- 12 Dec 2022 (actual)
- First posted
- 7 May 2020 (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.
Starting in late 2019, the world is facing a pandemic with the SARS-CoV-2 virus. Patients with end-stage kidney disease and on treatment with renal replacement therapy are high risk patients, as they are unable to maximize social distancing.
We plan to gather epidemiological data using two different diagnostic approaches. We will compare a symptom-driven screening, in combination with a nasopharyngeal swab plus computed tomography (clinical approach) against serological surveillance.
Detailed description
In late 2019, a cluster of patients with unexplained pneumonia was linked to a novel beta-coronavirus, now known as severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) 1. The world health organization subsequently has coined this disease as COVID-19. By the time the scientific community was alerted, the epidemiological data suggested that the virus had already spread to other regions of mainland China, as well as foreign cities with close transport links to the original epicenter 2. The world initially answered by divergent responses. Two months on, we are experiencing a devastating pandemic with local outbreaks across all continents.
As more and more patients arrive at the hospitals, our focus is drawn to the acute and the important issues, treating large numbers of patients in grave condition. The surge in patients requiring medical care may overwhelm even the most sophisticated healthcare systems 3. The approach adopted by almost all nations is to 'flatten the curve', i.e. to reduce peak demand of healthcare resources 4. While individual countries follow different paths, the common denominator is to maximize social distancing. The main goal is to reduce the basic reproduction number (R0) as much as possible, to ideally less than 1.
An overview of the clinical characteristics of confirmed cases in China alerted the world that young age does not protect against infection 5. Disease severity, however, varies by age with more elderly people becoming seriously ill, and by underlying medical condition(s) 6. The impact on peak medical demand thus will be even greater if we succeed in maximizing social distancing of the most vulnerable and most frail patients, those who are more likely to become seriously ill.
This is, however, difficult for dialysis patients who cannot self-isolate and cannot avoid multiple contacts per week with health care workers and other patients. While isolating dialysis patients and health care workers with a suspected SARS-CoV-2 infection is important to limit transmission of the virus, these measures are insufficient to avoid transmission since it is estimated that asymptomatic or paucisymptomatic people play a major role in the spread of the virus. So far, epidemiological data in patients on IHD during an SARS-CoV-2 outbreak are limited. A single case-series of cases from China has been reported in prepublication. 37 out of 230 patients were infected with SARS-CoV-2, of which 6 died (crude mortality rate 16.2%). The authors suggest that not all of these died directly from the consequences of COVID-19. However, adjudication of cause of death might differ in future case series.
The current gold standard for the diagnosis of acute respiratory syndrome due to SARS-CoV-2 (COVID-19) is the detection of viral RNA in respiratory tract samples. The sensitivity of a negative PCR result is, however, not 100%. False-negatives can occur, especially when using nasopharyngeal swabs (positivity rate estimated at 54%-74%) due to sampling error and in patients with low viral loads, especially in patients who present at day 8 or later and mild cases. While a CT scan can be a valuable tool in patients with a suspicion of COVID-9, measurement of antibodies against SARS-CoV-2 is the only reliable way to estimate the prevalence of SARS-CoV-2 infection since patients can be pauci-symptomatic or asymptomatic.
A number questions remain regarding the use of antibodies for epidemiologic studies and to determine immunity. Can someone have a colonization with SARS-CoV-2 without developing IgG antibodies? In this case, would this person be protected against reinfection? Doctors of the University of Bonn recently reported on April 9th (H. Streeck et al.,data not yet published) that only 15% of a sample of 1.000 inhabitants of the small town Gangelt, a local hotspot in North Rhine Westphalia tested positive for IgG antibodies. These data suggest that even in severely affected regions the critical threshold for herd immunity might not have been reached. This means that there is a significant risk of new outbreaks, particularly after schools might reopen later (maybe in summer 2020, and in fall 2020).
Given that dialysis patients are at the same time potentially more vulnerable to SARS-CoV-2 infection, and cannot self-isolate, it is important to closely monitor this group of patients. A second benefit of this population is that it easily accessible for blood sampling, and close clinical follow-up is ensured.
The aim of this study is to determine the prevalence of patients who were infected with SARS-CoV-2 by measuring IgG antibodies at different time points.
Trial objectives The aim of the current study is to collect epidemiological data of the incidence of severe acute respiratory syndrome Corona Virus type 2 (SARS-CoV-2) infections patients with end-stage kidney disease in a Belgian Hospital setting.
The objective is to compare two means of detection of infection, one symptom-driven surveillance and a second based on cross-sectional serology.
Primary endpoints Positive serology for SARS-CoV-2 at census date(s)
Secondary endpoints Detection of SARS-CoV-2 infection by symptom-driven surveillance
Trial Design Cross-sectional and longitudinal observational study of prevalent patients with end-stage kidney disease
Study design
- Observational model
- Cohort
- Time perspective
- Prospective
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| ESKD | – | Other: dialysisPatients with ESKD and on treatment with any form of dialysis |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
- Study population
- Patients with end-stage kidney disease (ESKD) receiving renal replacement therapy
Key inclusion criteria (4 listed)
- Patients with end-stage kidney disease (ESKD) receiving renal replacement therapy
- Age 18 years or older
- Treated at University Hospitals Leuven, or Jessa Ziekenhuis Hasselt
- Providing informed consent
Key exclusion criteria (2 listed)
- Refusal to provide informed consent
- Transfer to another dialysis unit
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 |
|---|---|---|
| dialysistreatment with dialysis. This can be hemodialysis, hemodiafiltration, peritoneal dialysis | Other | ESKD |
Primary outcome
Antibodies against SARS-CoV-2
Time frame: one year
serology to test for IgG and IgM antibodies against SARS-CoV-2
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 3 Jul 2024.
- Individual participant dataSharing planned: Undecided. 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. This study is not recruiting at the moment.
Bjorn Meijers, MD, PhD principal investigator
UZ Leuven
3 sites in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of SARS-CoV 2 and End Stage Renal Failure on Dialysis, run by Universitaire Ziekenhuizen KU Leuven at 3 sites in Belgium.
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 4 inclusion and 2 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: finished, as of the sponsor's last update on 3 Jul 2024. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 3 sites in Belgium. 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?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Antibodies against SARS-CoV-2 (time frame: one year). 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 3 Jul 2024.