Official Title
A Real World Study of Paxlovid for the Treatment of Hospitalized Patients Confirmed With COVID-19
Brief Summary

The study was designed to analyze the efficacy and safety of Paxlovid for the treatmentof COVID-19.

Detailed Description

The study is a real-world study and the case records of patients with COVID-19 who visit
Huashan Hospital affiliated to Fudan University from 2022 to 2027 and receive Paxlovid
therapy will be collected in this study. The medical data including patient demographic,
clinical characteristics, laboratory examination, history of treatments, adverse
reactions and treatment outcome will be extracted to analyze the effectivity and safety
of paxlovid and explore the prognosis-relevant factors of COVID-19.

Recruiting
COVID-19

Drug: Paxlovid

The study is a real-world study. According to the actual medical history of patients, the
usage of paxlovid will be collected.

Eligibility Criteria

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.

Eligibility Gender
All
Eligibility Age
Minimum: 12 Years ~ Maximum: N/A
Countries
China
Locations

Huashan Hospital Affiliated to Fudan University
Shanghai, China

Investigator: Jiming Zhang, M.D.
Contact: +86 021-52887948
jmzhang@vip.126.com

Contacts

Feng Sun, MD
+86 02152889999
aaronsf1125@126.com

Feng Sun, MD, Principal Investigator
Huashan Hospital affliatied to Fudan University

Huashan Hospital
NCT Number
Keywords
Paxlovid
MeSH Terms
COVID-19
Nirmatrelvir and ritonavir drug combination