A Study to Learn About the Patients With COVID-19 Prescribed Paxlovid in Morocco

Sponsor
Pfizer (Industry)
Overall Status
Not yet recruiting
CT.gov ID
NCT05997485
Collaborator
(none)
150
8

Study Details

Study Description

Brief 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.

Condition or Disease Intervention/Treatment Phase

Study Design

Study Type:
Observational
Anticipated Enrollment :
150 participants
Observational Model:
Cohort
Time Perspective:
Retrospective
Official Title:
A Retrospective Observational Non-Interventional Study (NIS) to Assess Patient Characteristics Among COVID-19 Patients Receiving Treatment With Nirmatrelvir/Ritonavir (PAXLOVIDTM) in Morocco.
Anticipated Study Start Date :
Oct 1, 2023
Anticipated Primary Completion Date :
Apr 30, 2024
Anticipated Study Completion Date :
May 31, 2024

Arms and Interventions

Arm Intervention/Treatment
Participants receiving Paxlovid Treatment

Patients administered oral Paxlovid as prescribed according to national Morocco treatment guidelines for Covid.

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

    Primary Outcome Measures

    1. Demographical Characteristics of Participants [Approximately 01 June 2022 through 30 June 2023]

    2. Clinical Characteristics of Participants [Approximately 01 June 2022 through 30 June 2023]

    3. Number of Participants with Pre-existing Comorbidites [Approximately 01 June 2022 through 30 June 2023]

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    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.

    Contacts and Locations

    Locations

    No locations specified.

    Sponsors and Collaborators

    • Pfizer

    Investigators

    • Study Director: Pfizer CT.gov Call Center, Pfizer

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Pfizer
    ClinicalTrials.gov Identifier:
    NCT05997485
    Other Study ID Numbers:
    • C4671060
    First Posted:
    Aug 18, 2023
    Last Update Posted:
    Aug 18, 2023
    Last Verified:
    Aug 1, 2023
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Keywords provided by Pfizer
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Aug 18, 2023