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NCT07720596

Molnupiravir and COVID-19 Mortality Reduction in the Omicron Era

Sponsor: Charles University, Czech Republic

View on ClinicalTrials.gov

Summary

This retrospective real-world target trial emulation uses complete Czech nationwide registry data to evaluate whether molnupiravir treatment is associated with lower COVID-19 mortality during the Omicron era. The study compares adults with confirmed acute COVID-19 treated with molnupiravir in addition to standard care versus matched controls treated with standard care without molnupiravir. Patients are followed for three months from time zero, and primary endpoints are the COVID-19 case fatality rate and all-cause mortality.

Official title: Effect of Molnupiravir on COVID-19 Mortality in the Omicron Era: A Real-World Target Trial Emulation Using Complete Czech Nationwide Data

Key Details

Gender

All

Age Range

20 Years - Any

Study Type

OBSERVATIONAL

Enrollment

1814551

Start Date

2022-01-01

Completion Date

2024-12-31

Last Updated

2026-07-22

Healthy Volunteers

No

Interventions

DRUG

Molnupiravir

800 mg of molnupiravir administered twice daily, i.e., four capsules every 12 hours for five days.

Locations (1)

Department of Pharmacology, Third Faculty of Medicine, Charles University

Prague, Czechia