Clinical Trials in China / NCT05387369
Recruiting
Observational
A Real World Study of Paxlovid for the Treatment of Hospitalized Patients Confirmed With COVID-19
NCT05387369 · tracked via the Priya Life Science China tracker
Condition(s) studied
COVID-19
Investigational drug(s) / intervention(s)
Paxlovid: The study is a real-world study. According to the actual medical history of patients, the usage of paxlovid will be collected.
Study summary
The study was designed to analyze the efficacy and safety of Paxlovid for the treatment of COVID-19.
Eligibility
Inclusion Criteria:
* Participants who have a positive SARS-CoV-2 test result;
* Participants who have one or more mild or moderate COVID-19 symptoms.
Exclusion Criteria:
* No specific exclusion criteria in this real world study.
Primary outcome measure(s)
- Viral shedding time — up to 28 days
time from the first positive testing to the first day of nucleic acid Ct value\> 35 for both ORF1ab and N gene (in two consecutive). - Percentage of the participants who have progression of COVID-19 — up to 28 days
Percentage of participants who experience these events by Day 28 Progress to severe and/or critical COVID-19; Death from any cause
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| Huashan Hospital Affiliated to Fudan University | Shanghai | China | Recruiting |
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Official registry record
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT05387369 on ClinicalTrials.gov ↗ ← All trials in China