- Disease: Post-COVID-19
- Study type: Randomised Clinical Trial, Treatment
- Study type descriptors: Interventional, Single centre
- Objective: To evaluate the efficacy of nirmatrelvir/ritonavir in providing sustained improvement in quality of life for non-hospitalized patients with post-acute COVID-19 syndrome
- Number of participants enrolled: 219
- Study enrolling from to
- Study includes follow-up for 90 days
Study Data
- Adults (18-64 years)
- General population
- Elderly (≥65 years)
- Outpatient clinic
- SARS-CoV-2
- Post-COVID-19
- Pharmacological intervention
- Antivirals
- Nirmatrelvir/Ritonavir
External Links
Other information
The information was provided with the aid of the study investigators
If you would like to contact the Principal Investigator of the study please email: ccb@ateneo.univr.it
The data is updated up to