Micronized/ultramicronized palmitoylethanolamide improves depression and fatigue in coronavirus disease 2019 (COVID-19) survivors
Observational studyHumans
- Design
- Observational study
- Subjects
- 98 COVID-19 survivors with neuropsychiatric symptoms at a Milan post-COVID clinic in 2021: 57 accepted treatment, 41 declined and served as the comparison
- Dose used in the study
- Micronised and ultramicronised palmitoylethanolamide 600 mg twice daily
- Duration
- 3 months
- What was measured
- Validated scales for depression, fatigue, chronic pain and subjective wellbeing before and after
What the authors reported
The treated group improved more in depression and fatigue (both p < 0.05) but not in chronic pain or wellbeing. Treatment predicted improvement after adjusting for age, sex and baseline status. Those with worse fatigue and wellbeing at baseline gained most.
Limits of this study
Patients who accepted treatment were compared with those who declined, which is not randomisation, and the authors call the study retrospective. No placebo, no blinding. Two of four outcomes did not differ. Authors declare no conflicts; registered NCT04318366.
Source
PubMed 38381905 · doi:10.1097/YIC.0000000000000537
Entry checked against the abstract on PubMed on 2026-09-22. The dose shown is the dose the researchers used. It is not a recommendation. How to read this page.