Official Title
Scripps-eMed Covid-19 Study: A Prospective Monitoring Study for Those Individuals Treated With Paxlovid
Brief Summary

A prospective monitoring study for those individuals treated with Paxlovid

Detailed Description

The purpose of this study is to understand the epidemiology and pathophysiology of
Paxlovid rebound in patients with acute Covid-19 infection who have been prescribed the
Paxlovid per standard of care.

The study will be a collaborative effort between Scripps and eMed, digitally recruiting
800 participants who have tested positive for Covid-19 and have agreed to be prescribed
Paxlovid on the eMed platform.

The vision of the study is to understand Paxlovid rebound and ultimately inform
management of acute Covid-19 infection.

Unknown status
COVID-19
Eligibility Criteria

Inclusion Criteria:

- Age > 18

- Covid positive

- Qualified for Paxlovid prescription (treatment decision already made prior to
enrollment)

Exclusion Criteria:

- Non-english speaking

- Resides outside of the United States

Eligibility Gender
All
Eligibility Age
Minimum: 18 Years ~ Maximum: N/A
Countries
United States
Locations

Scripps Research Institute
San Diego, California, United States

Jay Pandit, MD, Principal Investigator
Scripps Research Institute

NCT Number
Keywords
Paxlovid
Rebound
Covid-19
MeSH Terms
COVID-19