Covid-19 Infection in After Vaccination
NCT05033834 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 100
Last updated 2021-09-13
Summary
Coronavirus disease 2019 (COVID-19), caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), was first identified in Wuhan, China. It rapidly spread, resulting a global pandemic in March 2020. Globally, till 27 August 2021, there have been 214,468,601 confirmed cases of COVID-19, including 4,470,969 deaths, reported to WHO.
With the absence of curative treatment for COVID-19 infection the development of safe and effective vaccines is critical to ending the COVID-19 pandemic. The Pfizer/BioNtech Comirnaty vaccine was listed for WHO Emergency Use Listing (EUL) on 31 December 2020. The SII/Covishield and AstraZeneca/AZD1222 vaccines (developed by AstraZeneca/Oxford and manufactured by the State Institute of India and SK Bio respectively) were given EUL on 16 February. The Janssen/Ad26.COV 2.S developed by Johnson \& Johnson, was listed for EUL on 12 March 2021. The Moderna COVID-19 vaccine (mRNA 1273) was listed for EUL on 30 April 2021 and the Sinopharm COVID-19 vaccine was listed for EUL on 7 May 2021. The Sinopharm vaccine is produced by Beijing Bio-Institute of Biological Products Co Ltd, subsidiary of China National Biotec Group (CNBG). The Sinovac-CoronaVac was listed for EUL on 1 June 2021. As of 25 August 2021, a total of 4,953,887,422 vaccine doses have been administered. In large, randomized-controlled trials, vaccines were found to be safe and efficacious in preventing symptomatic, laboratory-confirmed COVID-19.
However, a small percentage of fully vaccinated persons will develop symptomatic or asymptomatic infections with SARS-CoV-2, the virus that causes COVID-19. A vaccine breakthrough infection is defined as the detection of SARS-CoV-2 RNA or antigen in a respiratory specimen collected from a person ≥14 days after receipt of all recommended doses of an FDA-authorized COVID-19 vaccine. A total of 10,262 SARS-CoV-2 vaccine breakthrough infections had been reported from 46 U.S. states and territories as of April 30, 2021. Among these cases, 6,446 (63%) occurred in females, and the median patient age was 58 years (interquartile range = 40-74 years). Based on preliminary data, 2,725 (27%) vaccine breakthrough infections were asymptomatic, 995 (10%) patients were known to be hospitalized, and 160 (2%) patients died.
Conditions
- Covid19
Interventions
- OTHER
-
covid-19 vaccines registered in Egypt
Astra Zeneka vaccine, Sinopharm vaccine, Sinovac vaccine, Jonson and Jonson vaccine, Spotnic V vaccine
Sponsors & Collaborators
-
Assiut University
lead OTHER
Eligibility
- Min Age
- 18 Years
- Max Age
- 80 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2021-11-01
- Primary Completion
- 2022-11-01
- Completion
- 2022-12-31
Countries
- Egypt
Study Locations
More Related Trials
-
Efficacy, Safety and Immunogenicity Study of SARS-CoV-2 Inactivated Vaccine
NCT04508075 ·Status: COMPLETED ·Phase: PHASE3
-
Immunogenicity and Safety Study of Self-amplifying mRNA COVID-19 Vaccine Administered With Influenza Vaccines in Adults
NCT06279871 ·Status: COMPLETED ·Phase: PHASE3
-
A Study to Learn About Flu and COVID-19 Vaccine Responses in Healthy People
NCT06683352 ·Status: COMPLETED ·Phase: PHASE1/PHASE2
-
A Study to Learn About a Combined COVID-19 and Influenza Shot in Healthy Adults
NCT06237049 ·Status: COMPLETED ·Phase: PHASE2
-
A Study Looking at the Effectiveness, Immune Response, and Safety of a COVID-19 Vaccine in Adults in the United Kingdom
NCT04583995 ·Status: COMPLETED ·Phase: PHASE3
-
Evaluate the Safety and Efficacy of Quadrivalent Influenza in Real-world Situations.
NCT06334510 ·Status: COMPLETED
-
Simultaneous mRNA COVID-19 and IIV4 Vaccination Study
NCT05028361 ·Status: COMPLETED ·Phase: PHASE4
-
Safety, Tolerability, and Immunogenicity of VAL-339851 in Healthy Adult Subjects
NCT03345043 ·Status: COMPLETED ·Phase: PHASE1
-
A Study to Evaluate the Safety, Tolerability, and Immunogenicity of a Combined Modified RNA Vaccine Candidate Against COVID-19 and Influenza.
NCT06178991 ·Status: COMPLETED ·Phase: PHASE3
-
Active Surveillance for Adverse Events Following Immunization With the Butantan Trivalent Influenza Vaccine (2018)
NCT03392207 ·Status: COMPLETED
-
Does Repeat Influenza Vaccination Constrain Influenza Immune Responses and Protection
NCT05110911 ·Status: ACTIVE_NOT_RECRUITING
-
Evaluation of Immunogenicity of COVID-19 Vaccine in Chinese Population
NCT06763887 ·Status: COMPLETED
-
This Study Intends to Describe the Characteristics of Patients Given the Pfizer-BioNTech Bivalent mRNA COVID-19 Vaccine and Any Commercially Available Influenza Vaccines at the Same Time Versus at Different Times.
NCT05858450 ·Status: COMPLETED
-
Safety and Immunogenicity of BNT162b2 Coadministered With SIIV in Adults 18 Through 64 Years of Age
NCT05310084 ·Status: COMPLETED ·Phase: PHASE3
-
COVID 19 Seroprevalence Amongst Healthcare Workers in JHAH
NCT04469647 ·Status: UNKNOWN
-
A Study to Learn About How the Flu and COVID-19 Vaccines Act in Healthy People
NCT06821061 ·Status: COMPLETED ·Phase: PHASE1/PHASE2
-
Covid-19 and Influenza Oral Vaccine Study
NCT06355232 ·Status: RECRUITING ·Phase: PHASE1
-
Evaluation of the Effectiveness of Vaccination With 2009 H1N1 Vaccines During Influenza Season 2010-11
NCT01206114 ·Status: COMPLETED
-
Heterologous Boost Immunization with Ad5-nCoV After Three-dose Priming with an Inactivated SARS-CoV-2 Vaccine
NCT05303584 ·Status: COMPLETED ·Phase: PHASE4
-
Safety and Immunogenicity of COVID-19 Vaccine Administered in Older Adults
NCT05012800 ·Status: UNKNOWN ·Phase: PHASE4
-
Prospective Monitoring of BNT162b2 Second Vaccination Booster Effects in Health Care Workers (HCW)
NCT05516459 ·Status: UNKNOWN
-
Study to Investigate the Immunogenicity, Reactogenicity, and Safety of mRNA-1083 Vaccine (SARS-CoV-2 [COVID-19] and Influenza) in Adults ≥50 Years of Age
NCT06694389 ·Status: COMPLETED ·Phase: PHASE3
-
Safety Study of Quadrivalent Subunit Influenza Vaccine in People Aged 3 Years and Older
NCT07332689 ·Status: COMPLETED
-
Safety and Immunogenicity of the Butantan Quadrivalent Influenza Vaccine
NCT03927131 ·Status: COMPLETED ·Phase: PHASE3
-
Study to Evaluate the Efficacy, Safety and Immunogenicity of Influenza Vaccine in Healthy Subjects (Aged 6 to <72 Months) Versus Control Vaccines
NCT00644059 ·Status: COMPLETED ·Phase: PHASE3