Trial ID: | L0847 |
Source ID: | NCT05624840
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Associated Drug: |
Nirmatrelvir/Ritonavir
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Title: |
Safety and Clinical and Virologic Outcomes in CKD Patients Treated With Nirmatrelvir-ritonavir
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Acronym: |
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Status: |
COMPLETED
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Study Results: |
NO
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Results: |
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Conditions: |
COVID-19|Chronic Kidney Disease stage4|Chronc Kidney Disease Stage 5
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Interventions: |
DRUG: Nirmatrelvir/ritonavir
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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
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Sponsor/Collaborators: |
Sponsor: Chinese University of Hong Kong
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Gender: |
ALL
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Age: |
ADULT, OLDER_ADULT
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Phases: |
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Enrollment: |
85
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Study Type: |
OBSERVATIONAL
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Study Designs: |
Observational Model: |Time Perspective: p
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Start Date: |
2022-11-07
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Completion Date: |
2023-02-01
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Results First Posted: |
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Last Update Posted: |
2024-02-07
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Locations: |
Prince of Wales Hospital, Chinese University of Hong Kong, Shatin, New Territories, SAR, Hong Kong
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URL: |
https://clinicaltrials.gov/show/NCT05624840
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