Evaluating Paxlovid for treating hospitalized COVID-19 patients

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational study aims to analyze the efficacy and safety of Paxlovid in hospitalized patients diagnosed with COVID-19. It will collect and review medical records of patients treated with Paxlovid at Huashan Hospital from 2022 to 2027, focusing on demographic data, clinical characteristics, laboratory results, treatment history, adverse reactions, and outcomes. The goal is to assess how effective Paxlovid is and identify factors that may influence the prognosis of COVID-19.

Why it matters

Who can join: the full rules

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.

Where it's running

• Huashan Hospital Affiliated to Fudan University
  Shanghai, China Recruiting

Study contacts

• Principal investigator: Feng Sun, MD — Huashan Hospital affliatied to Fudan University
• Study coordinator: Feng Sun, MD
• Email: aaronsf1125@126.com
• Phone: +86 02152889999

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.