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Vaccine RefusalVaccEffectNCT05069454

Study on COVID-19 Vaccine Effectiveness Among Health Workers in Azerbaijan

A study testing COVID-19 vaccine Observation of individuals who receive the COVID-19 vaccine in people with Vaccine Refusal and Covid19, run by Public health and reforms Center of Ministry of Health at 1 site in Azerbaijan.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
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Trial summary

Many critical questions remain about the effectiveness of COVID-19 vaccines in real-world settings. These questions can only be answered in post-introduction vaccine effectiveness studies. Read more about this study

Who is it for?
Ages 18 years and olderHealthy volunteers can take part
Conditions the study is for
Vaccine Refusal, Covid19
What is being tested?
COVID-19 vaccine Observation of individuals who receive the COVID-19 vaccine
Type of treatment
Vaccines
Could I receive a placebo?
No, everyone receives an active treatment
How many people
1,500 participants
Where
1 siteAzerbaijan
Study dates
10 May 2021to 20 Jul 2022
Phase
Interventional
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
  • Healthy volunteers accepted
  • Adult, Older adult

Who may be able to join

  • All Health Workers in selected 7 hospitals eligible to receive the COVID-19 vaccination.

Who cannot join

  • Health Workers who are not eligible for COVID-19 vaccination or have a contraindication to vaccination.
  • Health Workers who do not work at selected 7 hospitals.

Trial locations and contacts

1 site in 1 country.

Azerbaijan1 site, 1 recruiting
  • Public Health and Reforms Center of Ministry of Health

    Baku, AZ1122

    Nabil Seyidov, PhD, 994503492948, nabil.seyidov@isim.az

    Samir Mehdiyev, MPH, samir.mehdiyev@isim.az

    Recruiting

Other trials in Azerbaijan

About this study

Official title: Cohort Study to Measure COVID-19 Vaccine Effectiveness Among Health Workers in Azerbaijan

Many critical questions remain about the effectiveness of COVID-19 vaccines in real-world settings. These questions can only be answered in post-introduction vaccine effectiveness studies.

This protocol describes a prospective one-year cohort study of hospital-based HWs in Baku city of Azerbaijan to evaluate the effectiveness of COVID-19 vaccine in preventing laboratory-confirmed SARS-CoV-2 infection and COVID-19 disease. HWs are the target population in this study because HWs have been prioritized to be the first group to receive the vaccine in Azerbaijan and offer an early opportunity to evaluate the vaccine in a population in which it is critical that an effective vaccine be deployed.

Read more

HWs will be enrolled after the study protocol is approved by the local ethical review committee. All HWs eligible to be vaccinated with COVID-19 vaccine can be enrolled in the study, including those who intend to get vaccinated, those who don't plan on getting vaccinated, and those who are not sure. The target enrolment is 1500 HWs in six hospitals in Baku, the capital of Azerbaijan.

At enrolment, study participants will complete a baseline enrolment e-survey about demographics, clinical comorbidities, and work- and community-related behaviours related to infection risk. In addition, a baseline serology will be collected from participants at enrolment. No PCR testing for COVID19 virus will be done at the time of enrollment.

During the course of the study, participants will be actively followed for suspected symptomatic COVID-19 illness. Participants who meet a suspected case definition will be asked to have respiratory sample for SARS-CoV-2 by RT-PCR to be collected by trained HWs. PCR-positive samples from participants may also undergo genetic sequencing in or outside of Azerbaijan to identify the genetic makeup of the SARS-CoV-2 that caused the infection.

Finally, at 6 months and 12 months of the study, serology will be collected from participants to confirm and quantify the immunity after vaccination as a secondary objective. Serology will be tested for antibodies to SARS-CoV-2. Serology samples will be stored and may be sent to laboratories outside of Azerbaijan for advanced serologic testing.

Vaccine effectiveness should be analysed as described in the analysis section below.

In addition to the final analysis at the end of the one-year period, interim quarterly (every three months) analyses will be undertaken.

Read the detailed description
  1. Background and study rationale In late 2019 a novel severe acute respiratory syndrome - coronavirus 2 (SARS-CoV-2), which causes coronavirus disease 2019 (COVID-19), emerged. On January 30, 2020, WHO declared COVID-19 a public health emergency of international concern. On 11 March 2020, the World Health Organization declared COVID-19 a pandemic. The first case of COVID-19 was detected in Azerbaijan end of February, 2020, and since then 236,012 cases and 3,235 deaths has been reported in the country (data as of 8 March 2021).1

Effective and safe vaccines against COVID-19 are vital for controlling the pandemic. International collaborative efforts have accelerated the development of COVID-10 vaccines. As of 5 March 2021, there were 182 vaccines in pre-clinical development, and 79 vaccines in clinical development2. As of 18 February 2021, at least seven different vaccines across three platforms had been rolled out in countries, including the Coronac vaccine produced by Chinese company Sinopharm.

Evaluating the real-world COVID-19 vaccine performance is critical for understanding the risks and benefits of vaccination programs. Many factors impact real-world vaccine effectiveness (VE), including vaccine transportation and storage and how patients are vaccinated. In addition, the people who get the vaccine in clinical trials are often young and healthy, and therefore different from those who will receive vaccines in the real world. Post-licensing VE studies can also answer questions about effectiveness by age-group and underlying medical conditions, duration of vaccine protection, relative effectiveness of different vaccines, relative effectiveness of one dose vs. two doses, and effectiveness of the vaccine against new strains of SARS-CoV-2.

Health workers (HW) have been targeted for this study for a number of reasons. Azerbaijan has prioritized HWs for vaccination in line with the recommendations of the WHO SAGE and the European Technical Advisory Group on immunizations for use of COVID-19 vaccines when supply is limited. HWs provide a critical essential service in the COVID-19 pandemic response. HWs are at high risk of acquiring infection and associated morbidity and mortality, and also pose a risk of onward transmission to people who are also at high risk of serious COVID-19 outcomes. Ensuring that HWs receive an effective vaccine is also guided by the principle of reciprocity because HWs play critical roles in the COVID-19 response, working under intense and challenging conditions. Targeting HWs in this study offers an opportunity to determine the effectiveness of the vaccine in a population in which it is critical that an effective vaccine be deployed. While the HW population is not perfectly representative of the population of Azerbaijan, having an early understanding of the effectiveness of the vaccine in this population can inform decisions about vaccine use in the general population.

Immunization of HWs in Azerbaijan with Coronavac started in January 18, and the second dose has been administered to more than 60% of HWs by 15 March 2021. At the same time, it is estimated that 45-60% of health workers at the six target hospitals have received at least one dose and 60% of those have also received second dose of the vaccine.

Investigators propose to study the effectiveness of the COVID-19 vaccine in HWs in six selected hospitals in Baku city of Azerbaijan in order to answer critical questions about the real-world performance of COVID-19 vaccines in one of the key target groups for vaccination.

The stakeholders of this study include the following: Azerbaijan Republic Ministry of Health, The Public Health and Reforms Center of the Azerbaijan MOH, TABIB (which is subsidiary of Mandatory Health Insurance Agency of Azerbaijan that manages most hospitals in the country) health workers in the six hospitals and in Azerbaijan in general, the administration of the six study hospitals, and the World Health Organization.

2.1. Objectives 2.1.1. Primary objective To measure the effectiveness of COVID-19 vaccines against symptomatic laboratory-confirmed SARS-CoV-2 infection amongst hospital level health workers eligible for vaccination.

2.1.2. Secondary objectives

  • What is the effectiveness of Covid-19 vaccine in preventing any laboratory- confirmed SARS-CoV-2 infection, including symptomatic and asymptomatic infection, as measured by infection detected by PCR and serology?
  • How long does the COVID-19 vaccine confer protection against infection?
  • What is vaccine effectiveness (VE) by age?
  • What is VE by comorbidity?
  • What is the VE in people who have been previously infected with SARS-CoV-2 compared with those who were previously uninfected?
  • Does vaccine effectiveness vary by degree of exposure to COVID-19 patients in the hospital setting and physical distancing practices outside of the hospital?
  • Does vaccine effectiveness vary by new strains of SARS-CoV-2 that may emerge?
  1. Methods 3.1. Study setting and population

The study will be conducted among health workers working in six hospitals in different districts of Baku, the capital of Azerbaijan republic. The number of employees in each hospital is provided in the Table below.

Hospitals in Baku are chosen for a number of reasons. The Baku capital is the largest city in the country with over 3 million inhabitants. It has the largest hospitals in the country and the largest number of hospital-based HWs of any city in the country. Baku has been and still is at the forefront of fight with pandemic; the largest number of infections have occurred in Baku, and the largest number of COVID-19 patients requiring medical care are being treated in Baku hospitals. In addition, conducting the study in Baku will facilitate issues related to monitoring, supervision and logistics,. given the nation-wide quarantine-related restrictions and limitations to regional travel. Investigators selected a convenience samples of hospitals in various parts of Baku city.

The study population will be composed of HWs in the above hospitals, eligible for vaccination, with no contraindication to receive COVID-19 vaccine. HWs include all categories of staff working in these hospitals, including clinical and non-clinical/administrative staff and staff with direct patient interaction and those without direct patient interaction.

All HWs who are eligible for vaccination, according to MoH guidelines, will be offered enrolment, regardless of their intention to receive the COVID-19 vaccine. Currently, all HWs are eligible to receive vaccines unless they have contraindications, such as severe allergic reactions to previous vaccinations. Along with HWs, the educators, police and military personnel as well as all citizens >50 years of age are eligible to receive vaccines unless there are contraindications including allergies to vaccine incipient/excipients or previously confirmed allergic reaction to vaccination or current viral or bacterial infections.

This study will ensure follow up of enrolled participants via serology, respiratory swabs, and questionnaires. Participants may receive COVID19 vaccine during the study period but not as part of this study.

Efforts will be made to enroll all HW as close as possible to the time of their first vaccination.

Study staff will coordinate with hospital administration in order to ensure that the study will not interfere with vaccine administration.

Being tested
COVID-19 vaccine Observation of individuals who receive the COVID-19 vaccine
Medical subject headings
Vaccination Refusal, COVID-19

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • COVID-19 vaccine Observation of individuals who receive the COVID-19 vaccineBiological

    To measure the effectiveness of COVID-19 vaccines against symptomatic laboratory-confirmed SARS-CoV-2 infection amongst hospital level health workers eligible for vaccination.

Study groups in NCT05069454
Study groupRoleWhat they receive
Exposure groupActive comparatorHealthcare workers vaccinated by any of the available COVID19 vaccine;
Receives: Biological: COVID-19 vaccine Observation of individuals who receive the COVID-19 vaccine
Control groupActive comparatorHave not received any doses of any form of COVID-19 vaccine
Receives: Biological: COVID-19 vaccine Observation of individuals who receive the COVID-19 vaccine

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. COVID-19 vaccine effectiveness

    Weekly symptom questionnaire for all symptomatic vaccinated participants will identify potential new SARS-CoV-2 infection among vaccinated participants.

    Measured: 12 months

  2. Post-vaccination COVID-19 cases

    COVID-19 PCR testing for all symptomatic vaccinated participants will identify new SARS-CoV-2 infection among vaccinated participants.

    Measured: 12 months

Secondary outcomes (2)
  1. Vaccine effectiveness by age

    The enrollment questionnaire includes age of each participant. Data will be stratified by age at the time of analysis.

    Measured: 12 months

  2. Vaccine effectiveness in participants with various co-morbidities

    The enrollment questionnaire will assess the existence of specific co-morbidities among participants, including (but not limited to) heart disease, autoimmune disease, chronic liver disease and chronic kidney disease. Data will be stratified by co-morbidity at the time of analysis.

    Measured: 12 months

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted6 Oct 2021
  2. Study start10 May 2021
  3. Primary completion20 May 2022 (estimated)
  4. Study completion20 Jul 2022 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Prevention
Allocation
Non-randomised
Intervention model
Parallel groups
Model description
This is a prospective longitudinal cohort study, which will compare SARS-CoV-2 incidence among COVID-19 vaccinated and unvaccinated HWs who are eligible for COVID-19 vaccination in Azerbaijan. Upon approval of the protocol, all HWs working at six hospitals of Baku capital and who are eligible for COVID-19 vaccination will be offered to participate in the study and followed up regularly over time. The participation is completely voluntary.
Masking
None (open label)
Enrolment
1,500 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT05069454
Sponsor's protocol ID
2-PHRC-2021
Acronym
VaccEffect
Status last verified
Jul 2021
First submitted
10 Jun 2021
Last updated
6 Oct 2021
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Undecided

Questions about this trial

What is this clinical trial studying?

A study testing COVID-19 vaccine Observation of individuals who receive the COVID-19 vaccine in people with Vaccine Refusal and Covid19, run by Public health and reforms Center of Ministry of Health at 1 site in Azerbaijan.

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 1 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: status not confirmed, as of the sponsor's last update on 6 Oct 2021. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Azerbaijan. 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?

Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

Each site lists its own contact: choose the nearest one under Trial locations. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

COVID-19 vaccine effectiveness (time frame: 12 months). 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 6 Oct 2021.

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