Status: Finalised
First registered on:
01/04/2021
Last updated on:
09/01/2023
1. Study identification
EU PAS Register NumberEUPAS40404
Official titleCohort monitoring of Adverse Events of Special Interest and COVID-19 diagnoses prior to and after COVID-19 vaccination
Study title acronymECVM
Study typeObservational study
Brief description of the studyThis study will monitor AESI prior and following COVID-19 vaccination, with the purpose to estimate the incidence rates and pick up signals. This study will be conducted with funding from the EMA and in 4 data sources that have access to COVID-19 vaccine data and are able to rapidly update their data
Was this study requested by a regulator?Yes: EMA
Is the study required by a Risk Management Plan (RMP)?
Not applicable
Regulatory procedure number (RMP Category 1 and 2 studies only)
Other study registration identification numbers and URLs as applicable
2. Research centres and Investigator details
Coordinating study entity
Centre to which the investigator belongsUMCU
Department/Research groupData Science & Biostatistics
Organisation/affiliationUniversity Medical Center Utrecht
Details of (Primary) lead investigator
Title Professor
Last name Sturkenboom
First name Miriam
Is this study being carried out with the collaboration of a research network?
Yes
EU PE &PV
Other centres where this study is being conducted
Multiple centres
In total how many centres are involved in this Study?6
Countries in which this study is being conducted
International study
Italy
Netherlands
Spain
United Kingdom (Northern Ireland)
3. Study timelines: initial administrative steps, progress reports and final report
PlannedActual
Date when funding contract was signed15/12/2020
Start date of data collection15/02/202115/02/2021
Start date of data analysis30/03/2021
Date of interim report, if expected
Date of final study report30/11/202108/06/2022
4. Sources of funding
Please provide estimates of the percentage of funding by source for this study
Names(s)Approximate % funding
Pharmaceutical companies
Charities
Government body
Research councils
EU funding scheme
OtherEMA100
5. Contact details for enquiries
Scientific Enquiries
Title Professor
Last name Sturkenboom
First name Miriam
Address line 1Heidelberglaan 100
Address line 2
Address line 3
CityUtrecht
Postcode
CountryNetherlands
Phone number (incl. country code)31657831983
Alternative phone number
Fax number (incl. country code)
Public Enquiries
Title Professor
Last name Sturkenboom
First name Miriam
Address line 1Heidelberglaan 100
Address line 2
Address line 3
CityUtrecht
Postcode
CountryNetherlands
Phone number (incl. country code)31657831983
Alternative phone number
Fax number (incl. country code)
6. Study drug(s) information
Substance class (ATC Code)J07 (combinations)
7. Medical conditions to be studied
Medical condition(s)Yes
Coagulation disorders
Neurological disorders
Cardiovascular
Immunological
8. Population under study
Age
Preterm newborns
Term newborns (0-27 days)
Infants and toddlers (28 days - 23 months)
Children (2 - 11 years)
Adolescents (12 - 17 years)
Adults (18 - 44 years)
Adults (45 - 64 years)
Adults (65 - 74 years)
Adults (75 years and over)
Sex
Male
Female
Other population
Renal impaired
Hepatic impaired
Immunocompromised
Pregnant women
9. Number of subjects
Estimated total number of subjects5000000
10. Source of data
Is this study being carried out with an established data source?Yes
Data sources registered with ENCePP
Sources of data
Administrative database, e.g. claims database
Routine primary care electronic patient registry
11. Scope of the study
What is the scope of the study?
Risk assessment
Primary scope : Risk assessment
12. Main objective(s)
What is the main objective of the study?
To monitor the use and effects of COVID-19 vaccines
Are there primary outcomes?No
Are there secondary outcomes?No
13. Study design
What is the design of the study?
Cohort study
14. Follow-up of patients
Will patients be followed up?Yes
Please describe duration of follow up
Around 1-8 months
15. Data analysis plan
Please provide a brief summary of the analysis method
Risk estimation
16. ENCePP seal
Are you requesting the ENCePP seal for this study?
No
17. Full protocol
18. Study Results
Not submitted
Please list the 5 most relevant publications using data from your study
ReferenceLink to web-publication
Sturkenboom, MCJM, Messina, D, Paoletti, O, de Burgos, A, Garcia, P, Huerta Álvarez Consuelo, Llorente, A, Klungel, O, Martin, M, Martinez, M, Martin, I, Overbeek, J, Souverein, P, Swart, K, & Gini, R. (2022). Cohort monitoring of Adverse Events of Special Interest and COVID-19 diagnoses prior to and after COVID-19 vaccination (1.0). Zenodo. https://doi.org/10.5281/zenodo.6762311https://doi.org/10.5281/zenodo.6762311
Cohort monitoring of 29 Adverse Events of Special Interest prior to and after COVID-19 vaccination in four large European electronic healthcare data sources
Miriam CJM Sturkenboom, Davide Messina, Olga Paoletti, Airam Burgos Gonzalez, Patricia Garcia-Poza, Ana Llorente- Garcia, Consuelo Huerta, Mar Martin-Perez, Ivonne Martin, Jetty Overbeek, Marc Padros-Goossens, Patrick Souverein, Karin Swart-Polinder, Olaf Klungel, Rosa Gini
medRxiv 2022.08.17.22278894; doi: https://doi.org/10.1101/2022.08.17.22278894https://www.medrxiv.org/content/10.1101/2022.08.17.22278894v1
19. Other relevant documents
Conflict(s) of interest of
investigator(s)Not submitted
Composition of Steering Group and
ObserversNot submitted
Other documentsNot
submitted
Signed Code of
Conduct Checklist
Not submitted
Signed Code of Conduct Declaration
Not submitted
Signed Checklist for Study
Protocols
Not submitted
