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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT05997485
Other study ID # C4671060
Secondary ID
Status Withdrawn
Phase
First received
Last updated
Start date March 30, 2024
Est. completion date June 30, 2024

Study information

Verified date March 2024
Source Pfizer
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The purpose of this study is to collect information on the: - general information of a group of people such as their age, sex, and other facts. - clinical information of the patients such as any other illness before having COVID 19. In adult patients with COVID-19 who have been prescribed nirmatrelvir and ritonavir treatment. This study will be conducted in Morocco. The study will capture information of the adult COVID-19 outpatients and inpatients who have been prescribed nirmatrelvir, ritonavir treatment. The inpatients will be admitted in the hospital for other reasons than COVID-19. This study will have about 150 patients. The study will involve collection of patient information from medical records. The information collected can be either from papers or from computers. The study will include patient information of those who: - are confirmed to have COVID-19 infection during the study period from 01 June 2022 to 30 June 2023. - are 18 years of age or older. - are prescribed Nirmatrelvir and ritonavir. This study will help to inform decision-making on use of Paxlovid at the national level.


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date June 30, 2024
Est. primary completion date June 30, 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Confirmed COVID-19 infection during the study period from 01 June 2022 to 30 June 2023 - Nirmatrelvir, ritonavir written prescription Exclusion Criteria: - There are no exclusion criteria for this study.

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Nirmatrelvir/Ritonavir
Patients administered oral Paxlovid as prescribed according to national Morocco treatment guidelines for Covid.

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Pfizer

Outcome

Type Measure Description Time frame Safety issue
Primary Demographical Characteristics of Participants Approximately 01 June 2022 through 30 June 2023
Primary Clinical Characteristics of Participants Approximately 01 June 2022 through 30 June 2023
Primary Number of Participants with Pre-existing Comorbidities Approximately 01 June 2022 through 30 June 2023
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