Clinical Trial Details
— Status: Completed
Administrative data
| NCT number |
NCT05074017 |
| Other study ID # |
COVAG study protocol 2.0 |
| Secondary ID |
|
| Status |
Completed |
| Phase |
|
| First received |
|
| Last updated |
|
| Start date |
February 1, 2021 |
| Est. completion date |
March 31, 2021 |
Study information
| Verified date |
October 2021 |
| Source |
Synlab Holding Deutschland GmbH |
| Contact |
n/a |
| Is FDA regulated |
No |
| Health authority |
|
| Study type |
Observational
|
Clinical Trial Summary
The aim of the COVAG study (Covid-19 Antigen study) is to assess the diagnostic efficacy of
two of the most used rapid antigen tests (Roche & Abbott).
The study will be performed at the Corona Test Center Stuttgart Cannstatter Wasen.
Approximately 2000 patients will be enrolled after having signed the Informed Consent Form
(ICF). Each patient will receive 3 nasopharyngeal swabs. Two for the rapid antigen tests from
Roche and Abbott and one for the RT-PCR. Furthermore an anamnesis, short clinical examination
and blood draw is done. The blood is examined for SARS-CoV-2 antibodies and basic laboratory
tests to be communicated to participants.
Description:
1. Background:
Coronavirus disease 2019 (COVID-19) has quickly spread worldwide from Wuhan (China)
since December 2019. Reliable diagnostic technologies are pivotal to the fight against
COVID-19. While real-time reverse transcriptase-polymerase chain reaction (rRT-PCR)
based testing of respiratory specimens remains the gold standard for COVID- 19
diagnostics, several commercial assays for antibodies against (SARS-CoV-2) have emerged
during the previous months (Stocking et al., 2020).
Measuring the presence or absence of viral proteins (antigens), antigen tests may
provide results diagnosing an active SARS-CoV-2 infection much faster than RT-PCR or
equivalent tests. It has been argued that antigen tests may have a lower sensitivity
than RT-PCR or equivalent RNA-based tests, and as a result they are much more likely to
give false-negative results in individuals with lower amounts of virus. This may
possibly make them unreliable in individuals with an asymptomatic course of the disease,
in individuals in the first days of infection, and later than 5-7 days after onset of
symptoms (SYNLAB press release, 22.09.2020).
2. Objective:
The objective of this non-interventional study is to demonstrate that rapid antigen
tests for SARS-CoV-2 (Abbott and Roche) provide fast results and perform equally well
than RT-PCR, at least in symptomatic patients with high viral loads.
3. Study Design:
The study will be performed in at the Corona Test Center Stuttgart Cannstatter Wasen
operated by Dr. med. Hans-Jörg Wertenauer, Stuttgart, in close collaboration with the
SYNLAB MVZ Leinfelden-Echterdingen GmbH. Approximately 2000 patients will be enrolled at
after having signed the Informed Consent Form (ICF). Upon a scheduled study duration of
eight weeks, the investigators will be able to collect the required 2000 samples (50
patients per day).
One study visit is planned for data and blood collection (15,5 ml), antigen tests,
RT-PCR, serological tests, basic laboratory tests to be communicated to participants,
and ancillary blood tests (incriminated to be related to COVID-19 like inflammatory
markers, and micronutrients and vitamins). These will be performed at the at the SYNLAB
MVZ Leinfelden GmbH. Aliquots of the materials collected will be stored -20 degrees for
control measurements and ancillary tests, maximally for one year after the last patient
was enrolled into the study.
4. Rationale:
In the past weeks, there has been much discussion about rapid antigen tests for SARS-
CoV-2. The most recent generation of these tests, available from several different
suppliers, are expected to perform well in patients with high viral loads. This is
usually the case approximately 3-10 days after infection with the virus, when the person
is contagious, and may be asymptomatic or in the first days of symptoms.
It is therefore hoped that rapid antigen tests can support diagnosis of COVID-19 in
people who have the first symptoms. In the USA, some tests have received authorization
for diagnostic testing in symptomatic individuals, within 5-7 days from the onset of
symptoms (3).
5. Risks and benefits:
Three nasopharyngeal swabs and one blood sample will be obtained from each of the
participants. Antigen tests, RT-PCR and serological and ancillary laboratory tests are
performed in this study.
Risks from nasopharyngeal swabs: The biggest risk is discomfort. Rarely - 1 in thousands
- the person receiving the swab passes out from being super sensitive or gets a mild
nosebleed.
Risks from blood draw: The risks of venipuncture include being the most common reaction.
Significant complications (defined as cellulitis, phlebitis, diaphoresis, hypotension,
near syncope, syncope) are observed in Minor bruising at the site where the blood is
taken and hematoma (12 % approximately), with minor bruising approximately 3.5% of
patients. The most frequent single significant complication is hypotension at a
frequency occurred of approximately 2.6%. Syncope is seen in less than 1% of patients.
Other serious local reactions such as cellulitis or phlebitis are very rare (Galena HJ,
J. Fam. Pract. 1992 May;34(5):582-4). Blood sampling is therefore conducted in each of
the study sites under the surveillance of a board licensed physician.
Benefits to public health: Point of care antigen testing is an integral component of the
current national testing strategy serving for preventing of the spread of COVID 19
https://www.bundesgesundheitsministerium.de/fileadmin/Dateien/3_Downloads/C/C
oronavirus/Nationale_Teststrategie_kurz_041220.pdf There is, however, significant
uncertainty as to the reliability of antigen testing in comparison to the gold standard
of testing, rt-PCR. To the authors ́ knowledge a prospective, sufficiently sizeable and
challengeable evaluation of antigen testing under practice conditions has not been
completed so far. The current study is intended to close this gap. Its results are
urgently required and will have immediate impact on current recommendations for using
antigen testing. In particular, it will demonstrate weaknesses and strengths of antigen
testing and will allow to outweigh potential technical limitations of antigen testing
compared to rt-PCR against the advantage of short-term availability of test results.
Further, the thorough recording of the clinical health status and the basic laboratory
analysis performed in this study, it will be able to get further insights into clinical
predictors for the susceptibility for COVID 19.
Benefits to the individual. Participants will benefit in two ways. Other than with
rt-PCR, they will obtain the results of the antigen testing at once and on-site. In
addition, offering two antigen tests simultaneously, the results of the point-of-care
testing will be even more reliable than the result of a single test. Further, the
participants are offered a free of charge basic laboratory health check including the
following actionable health markers: basic blood cell count, C-reactive protein, HbA1c,
cholesterol, triglycerides, LDL cholesterol, HDL cholesterol,
gamma-glutamyl-transferase, creatinine along with formula-derived creatinine, vitamin D.
The investigators conclude that benefits of this study to the healthcare system which is
faced with the life-threatening and to the individual study participants clearly
outweigh the minor and manageable risks.
6. Population:
The investigators will include approximately 2000 consecutive male and female patients aged
18 years or above attending the Corona Test Center Stuttgart Cannstadter Wasen, in whom RT-
PCR testing for SARS-CoV-2 is medically indicated or requested.
6.1 Inclusion Criteria:
Subjects eligible for inclusion in this study must meet the following criteria:
1. Signed informed consent must be obtained prior to study participation. The patient must
be capable of understanding the nature, significance and implication of the trial.
2. Age 18 years or more
6.2 Exclusion criteria:
1. Lack of informed consent
2. Inability to understand the nature, significance and implication of the trial.
3. Severe clinical conditions requiring emergency hospitalization
4. Children and adolescents under the age of 18 years
7. Informed consent procedures Eligible subjects may only be included in the study after
providing IRB/IEC-approved informed consent. Informed consent must be obtained before
performing any study- specific procedures (Appendix 2).
8. Assessment schedule and assessments:
Informed Consent Form, Collection of demographic data and X relevant Medical History
SARS-CoV-2 Rapid Antigen Test (Roche), PANBIO Covid-19 Ag Rapid Test (Abbott), RT-PCR
Serological test (blood sample, 15,5 ml) Ancillary testing 8.1 Demographics, Medical history,
sampling: Patient demographic data and other characteristic data to be collected on all
patients include sex, age, weight, height, relevant medical history, vital signs and symptoms
characteristic of COVID-19 including precise time specifications for onset of symptoms.
No information about medication will be collected. Three independent nasopharyngeal swabs
will be obtained following standard procedures To avoid any bias due to the sequence of
taking the nasopharyngeal swabs, the investigators will randomly allocate the patients to
three sampling groups Group 1: RT-PCR - Antigen Test Roche - Antigen Test Abbott Group 2:
Antigen Test Roche - Antigen Test Abbott - RT-PCR Group 3: Antigen Test Abbott - RT-PCR -
Antigen Test Roche
The assignment of patients to each of these groups will be clearly specified on the case
record forms. There will be two forms for each patient:
Form 1: Routine analysis request sheet as used by the collection point for patient
identification which will be labelled with a bar code carrying the study number of a patient
Form 2: Study specific form containing a copy of the bar code with the study number, initials
of the patient and the year of birth.
8.2 SARS-CoV-2 Rapid Antigen Test (Roche): The SARS-CoV-2 Rapid Antigen Test is a rapid point
of care chromatographic immunoassay for the qualitative detection of specific antigens of
SARS-CoV-2 present in the human nasopharynx.
8.3 PANBIO Covid-19 Ag Rapid Test (Abbott): Panbio COVID-19 Ag Rapid Test Device is an in
vitro diagnostic rapid test for the qualitative detection of SARS-CoV-2 antigen (Ag) in human
nasopharyngeal swab specimens.
8.4 RT-PCR: RT-PCR evaluates the presence or absence of the SARS-CoV-2 genome in samples from
nasopharyngeal and oropharyngeal swabs and will be conducted according to the protocols
established at the SYNLAB MVZ Leinfelden GmbH.
8.5 Serological and ancillary testing: Blood samples (10 ml heparin plasma and 5.5 ml EDTA
plasma) will be collected to detect the presence of antibodies (specific immune response)
against SARS-CoV-2 antigenic proteins (e.g. Roche, Abbott). Specifically, all participants
will be offered to receive the results for the following analytes in acknowledgment of their
participation in the study: blood cell count, C-reactive protein, HbA1c, cholesterol,
triglycerides, LDL cholesterol, HDL cholesterol, gamma-glutamyl-transferase, creatinine along
with formula-derived creatinine, vitamin D. Backup samples will be collected to determine
ancillary parameters like inflammatory markers, and micronutrients and vitamins.
9. Observation Period:
NIS schedule:
Start of the patient recruitment: February 1, 2021 End of the observation period: March 31,
2021 Final report: May 31, 2021
10.Data analysis and statistical methods: A database of the pseudonymized data and results
will be generated. The investigators hypothesize that each of the antigen tests has a
sensitivity and specificity of 1.0 in relation to RT-PCR which will be considered as the
reference test. A p value of less than 0.05 will be required to consider each of the two
rapid tests equivalent to RT-PCR.
With the aid of power calculations for chi-square tests for two degrees of freedom, required
type I error probability equal to 0.05, required (1-type II error probability)equal to 0.8
and required effect size equal to 0.1 (small effect size in the sense of (4)) the
investigators obtain a number of at least N=964 observations for consecutive testing of
incoming patients in order to fulfill our requirements on significance and power to answer
the first research question. Because of the expected number of around 10% positive out of
1000 cases, the assumption of a chi-square distribution is permissible.
The investigators will also address the question whether different pre-test probabilities
will affect the sensitivity of the of the antigen tests. The investigators expect two major
indication groups with different pre-test probabilities contributing approximately 90 percent
of the rt-PCR positive samples: a) participants admitted for rt-PCR testing by a physician b)
participants seeking for rt-PCR testing upon recommendation my health care
authorities/contact persons. A total of approximately 200 rt-PCR samples will be required to
detect a statistically significant difference between these two groups at a type 1 error of
0.05 and a statistical power of 0.80. To answer this second question, the investigators will
extend the study to 2000 participants.
11. Ethics: The study protocol will be submitted to the Ethics Committee the Medical Faculty
Mannheim, University of Heidelberg and the study will not begin until written permission is
obtained. The study will be conducted in accordance with German law, EU Clinical Trial
regulations and the Declaration of Helsinki on the ethical principles of clinical research.
11.1 Patient information and Informed Consent: The objective, nature and extent of the
document must be explained in writing to every patient before he or she is included in the
study (Appedix 1). The patient must not be included unless he or she has given written
consent (Appendix 2). Patients will have the right to refuse to participate or to withdraw
from the study for any reason and at any stage without affecting the quality or accessibility
of their health care.
11.2 Data protection: The patient data collected for the study will be recorded in a
pseudonymised form (Appendix 4), with a patient number that cannot be attributed to the
identity of the patient. In the event of the study results being published, the personal data
may only be used if the patient's anonymity is upheld. The patient's data is guaranteed to be
always absolutely protected.
