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A Study to Learn About Effects of Living With COVID-19 and the Use of the Medicines Nirmatrelvir-Ritonavir in Treating COVID-19.

Pfizer logo

Pfizer

Status

Completed

Conditions

COVID-19

Treatments

Drug: SoC
Other: Disease description

Study type

Observational

Funder types

Industry

Identifiers

NCT06085924
NCT06085924 (Registry Identifier)
C4671061

Details and patient eligibility

About

The purpose of this study is to learn about:

  • effects of living with COVID-19 and
  • how effective is nirmatrelvir-ritonavir in treating COVID-19.

This is a study of two groups of COVID-19 patients in Taiwan.

In Group 1 the below participants were included in the study:

  • Patients of all ages.
  • Patients who were confirmed to have COVID-19 infection between 01 January 2021 and 31 December 2021.
  • Cases of patients registered in the databases.

In Group 2 the below participants were included in the study:

  • Participants who are 12 years or older.
  • Confirmed to have COVID-19 between 01 January 2022 and 31 December 2022.

Nirmatrelvir-ritonavir is taken by mouth and is used to treat COVID-19.

The study will look at:

  • the nature of Covid-19 disease.
  • as well as the experiences of people receiving the nirmatrelvir-ritonavir.

This study will help to:

  • understand what type of patients will need to be admitted to hospitals.
  • see severe results due to COVID 19 infection.
  • have more knowledge on the use of nirmatrelvir/ritonavir on COVID-19.

Enrollment

8,252,912 patients

Sex

All

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Cohort 1:

Inclusion Criteria:

  • Patients of all ages
  • Patients with a diagnosis of COVID-19 infection between 01 January 2021 and 31 December 2021
  • Cases of patients registered in the databases

Exclusion Criteria:

  • Patients without COVID-19 diagnosis

Cohort 2:

Inclusion Criteria:

  • ≥12 years of age
  • Have COVID-19 diagnosis with international classification of diseases (ICD) code between 01 January 2022 and 31 December 2022

Exclusion Criteria:

  • Patients without COVID-19 diagnosis

Trial design

8,252,912 participants in 2 patient groups

Cohort 1 - Cases of patients registered in the databases of all ages
Description:
Patients with a diagnosis of COVID-19 infection between 01 January 2021 and 31 December 2021
Treatment:
Other: Disease description
Cohort 2 - Cases of patients registered in the databases of ≥12 years of age
Description:
Have COVID-19 diagnosis with international classification of diseases (ICD) code between 01 January 2022 and 31 December 2022
Treatment:
Drug: SoC

Trial contacts and locations

1

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Central trial contact

Pfizer CT.gov Call Center

Data sourced from clinicaltrials.gov

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