← Human Trials & Peer-Reviewed Studies
Ultramicronized Palmitoylethanolamide and Luteolin Supplement Combined with Olfactory Training to Treat Post-COVID-19 Olfactory Impairment: A Multi-Center Double-Blinded Randomized Placebo- Controlled Clinical Trial.
Plain-language guide to PMID 35450527 (2022): double-blind randomized controlled trial of Copper (Supplement).
Key Facts
- PMID
- 35450527
- Journal
- Current neuropharmacology
- Year
- 2022
- Study type
- Randomized Controlled Trial
- Authors
- Di Stadio A et al. (15 authors)
- DOI
- 10.2174/1570159X20666220420113513
What This Study Did, in Plain Language
What Was Tested
Researchers studied Copper (Supplement) in this randomized controlled trial publication.
To investigate recovery of olfactory function in patients treated with PEA-LUT oral supplements plus olfactory training versus olfactory training plus placebo.
Sniffin' Sticks assessments were used to test the patients at baseline and 90 days.
Why It Was Studied
Olfactory training is the only evidence-based treatment for post-viral olfactory dysfunction.
Smell disorders after SARS-CoV-2 infection have been attributed to neuroinflammatory events within the olfactory bulb and the central nervous system.
Who Took Part
Eligible subjects had prior COVID-19 and persistent olfactory impairment >6 months after follow-up SARS-CoV-2 negative testing, without prior history of olfactory dysfunction or other sinonasal disorders.
How the Study Was Run
In design terms this was a randomized, double-blind, placebo-controlled and multicenter study.
Because people in this Copper (Supplement) study were split into groups at random, differences between the groups are less likely to reflect who happened to join each one.
Neither the participants nor the staff measuring them knew who was on Copper (Supplement), so expectations could not easily colour the readings.
A placebo (an inactive look-alike) gave the Copper (Supplement) group a baseline to be compared against.
Running at several centres spread the Copper (Supplement) study over different clinics and patient groups.
Multicenter double-blinded randomized placebo-controlled clinical trial was held.
What Was Measured
Topics PubMed links to this paper include Amides, COVID-19, Dietary Supplements, Ethanolamines, Luteolin, Olfaction Disorders and Palmitic Acids.
The authors tagged it with the keywords SARS-CoV-2, anosmia, anti-inflammatory, coronavirus, hyposmia and olfactory dysfunction.
What This Means in Plain Language
The paper is a randomized, double-blind and placebo-controlled study of Copper (Supplement).
Results are reported in around 5 sentences of the abstract; we leave them to the paper itself rather than summarise them.
The publication is from 2022 (Current neuropharmacology), a journal based in United Arab Emirates.
More context: the Copper (Supplement) compound page, all human trials.
Our Notes on the Compound
Copper (Supplement): The active site of cytochrome c oxidase is described as containing copper ions that are essential for electron transfer.
Related Pages
Source: PubMed record. This explanation is written by PeptideWhiz from the public record. For research and education only. Not medical advice; no dosing information is given.