A Study of COVID-19 Patients Receiving Treatment With Nirmatrelvir; Ritonavir in the Kingdom of Saudi Arabia
NCT ID: NCT06016556
Last Updated: 2025-06-05
Study Results
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View full resultsBasic Information
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COMPLETED
250 participants
OBSERVATIONAL
2023-10-17
2024-04-09
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
RETROSPECTIVE
Study Groups
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Patients receiving Nirmatrelvir; Ritonavir (PAXLOVID)
Adult COVID-19 patients' HCRU within the 30-day period following nirmatrelvir, ritonavir prescription.
nirmatrelvir, ritonavir
single cohort
Interventions
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nirmatrelvir, ritonavir
single cohort
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* Nirmatrelvir, ritonavir written prescription
Exclusion Criteria
18 Years
ALL
No
Sponsors
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Pfizer
INDUSTRY
Responsible Party
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Principal Investigators
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Pfizer CT.gov Call Center
Role: STUDY_DIRECTOR
Pfizer
Locations
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King Faisal Specialist Hospital & research center - Jeddah
Jeddah, , Saudi Arabia
King Abdulaziz Medical City
Riyadh, , Saudi Arabia
King Faisal Specialist Hospital and Research Center
Riyadh, , Saudi Arabia
Countries
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Provided Documents
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Document Type: Study Protocol
Document Type: Statistical Analysis Plan
Related Links
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To obtain contact information for a study center near you, click here.
Other Identifiers
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NCT06016556
Identifier Type: REGISTRY
Identifier Source: secondary_id
C4671054
Identifier Type: -
Identifier Source: org_study_id
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