- Disease: Post-COVID-19
- Study type: Randomised Clinical Trial, Treatment
- Study type descriptors: Interventional, Single centre
- Objective: To evaluate the effects of dietary supplementation with a pre-probiotic on patient-reported outcomes and clinician-reported outcomes in patients with post-COVID fatigue syndrome
- Number of participants enrolled: 32
- Study enrolling from to
- Study includes follow-up for 3 months
Study Data
- Adults (18-64 years)
- General population
- Elderly (≥65 years)
- SARS-CoV-2
- Post-COVID-19
- Non pharmacological intervention
- Dietary
- Probiotic
External Links
Other information
Funders/Sponsors:
- Provincial Secretariat for Higher Education and Scientifc Research, Germany
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