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Clinical Trial Details

Trial ID: L0847
Source ID: NCT05624840
Associated Drug: Nirmatrelvir/Ritonavir
Title: Safety and Clinical and Virologic Outcomes in CKD Patients Treated With Nirmatrelvir-ritonavir
Acronym:
Status: COMPLETED
Study Results: NO
Results:
Conditions: COVID-19|Chronic Kidney Disease stage4|Chronc Kidney Disease Stage 5
Interventions: DRUG: Nirmatrelvir/ritonavir
Outcome Measures: Primary: adverse event, Adverse events during or after treatment with nirmatrelvir-ritonavir (starting on or before day 30), serious adverse events and adverse events leading to discontinuation of nirmatrelvir-ritonavir, 30 days | Secondary: RAT, Time to negative rapid antigen test result, 30 days|Rebound, Rebound of positive rapid antigen test or polymerase chain reaction PCR up to day 30, 30 days|WHO Clinical Progression Scale CPS, Time to progression to CPS 5 up to day 30, 30 days|Symptoms, Time to resolution of symptoms, 30 days|Symptomatic rebound, Symptomatic rebound (symptomatic again after resolution of symptom with positive RAT or PCR), 30 days
Sponsor/Collaborators: Sponsor: Chinese University of Hong Kong
Gender: ALL
Age: ADULT, OLDER_ADULT
Phases:
Enrollment: 85
Study Type: OBSERVATIONAL
Study Designs: Observational Model: |Time Perspective: p
Start Date: 2022-11-07
Completion Date: 2023-02-01
Results First Posted:
Last Update Posted: 2024-02-07
Locations: Prince of Wales Hospital, Chinese University of Hong Kong, Shatin, New Territories, SAR, Hong Kong
URL: https://clinicaltrials.gov/show/NCT05624840