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OpenTrials
Completed

NCT Number: NCT05037227

Safety Profile Following Inactivated COVID-19 Vaccine in Healthy Adults Aged >18 Years in Indonesia

The aim of this study is evaluating safety profile of COVID-19 Vaccine in healthy adults aged >18 years in Indonesia.

Completed

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Key information

Conditions

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Jakarta Provincial Ministry of Health

Jakarta, DKI Jakarta, Indonesia

About this study

To assess any serious systemic reaction within 30 minutes after COVID-19 vaccine immunization.

To assess systemic reaction after COVID-19 Vaccine immunization. To assess local reaction after COVID-19 Vaccine immunization. To assess any serious adverse event after COVID-19 Vaccine immunization.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Clinically healthy adults aged > 18 years.
  • Subjects have been informed properly regarding the study and signed the informed consent form.
  • Subjects will commit to comply with the instructions of the investigator and the schedule of the trial.

Exclusion criteria

  • Subjects concomitantly enrolled or scheduled to be enrolled in another trial.
  • Evolving mild, moderate or severe illness, especially infectious disease or fever (body temperature ≥37.5℃, measured with thermometer).
  • Women who are lactating, pregnant or planning to become pregnant during the study period.
  • History of uncontrolled coagulopathy or blood disorders contraindicating intramuscular injection.
  • Subjects who have any history of confirmed or suspected immunosuppressive or immunodeficient state, or received in the previous 4 weeks a treatment likely to alter the immune response (intravenous immunoglobulins, blood-derived products or long-term corticosteroid therapy (> 2 weeks)).
  • Subjects receive any vaccination within 1 month before and after IP immunization.
  • Subjects plan to move from the study area before the end of study period.

Treatment and study plan

Primary outcomes

  1. Any serious adverse event occurring from inclusion until 30 minutes after the injection

    Time frame: Within 30 minutes after vaccination

    Number and percentage of subjects with serious systemic reactions 30 minutes after immunization.

Secondary outcomes

  1. Local reaction and systemic events occurring within 30 minutes after each immunization.

    Time frame: Within 30 minutes after vaccination

    Number and percentage of subjects with at least one of these adverse events, solicited or not, within 30 minutes after vaccination.

  2. Local reaction and systemic events occurring within 28 days after immunization

    Time frame: 28 days

    Number and percentage of subjects with at least one of these adverse events, solicited or not, within 28 days after vaccination.

  3. Any serious adverse event during observation period.

    Time frame: 28 days

    Number and percentage of subjects with serious adverse event from inclusion until 28 day after vaccination.

Sponsors and collaborators

Lead sponsor

PT Bio Farma

Industry

Registry information

Important dates

Study start
2021
Primary completion
2021
Study completion
2021
First posted
Sep 8, 2021
Registry last updated
Jul 27, 2022

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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