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Adverse events following COVID-19 vaccination

Adverse events following COVID-19 vaccination in a tertiary care hospital

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2021/04/032823
Enrollment
500
Registered
2021-04-15
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Control Intervention1: NIL: NIL

Sponsors

Dr Chandralekha N
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: All health care workers both males and females of age more than 18 years including doctors, nurses, allied health science staff, paramedicals, students, clerical staff, support staff of FMCI who have voluntarily received 1st and 2nd dose of Covid-19 vaccination and who consent to give information about Covid -19 vaccine adverse events

Exclusion criteria

Exclusion criteria: Covid-19 vaccinated health care worker not willing to provide any adverse event information following Covid-19 vaccination

Design outcomes

Primary

MeasureTime frame
We are looking for ADRs like fever, head ache, myalgia, nausea, vomiting, diarrhea, pain abdomen, sore throat, cough, dizziness, injection site pain etcTimepoint: 0-12 months -data collection 13-18 months- data analysis 18-24 months - publication—

Secondary

MeasureTime frame
recommendations will be made on the basis of primary outcomesTimepoint: 0-12 months -data collection 13-18 months- data analysis 18-24 months - publication—

Countries

India

Contacts

Public ContactDr Chandralekha N

Father Muller Medical College, Mangalore

smilekha25@fathermuller.in9743701662

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026