Clinical Trials Directory

Trials / Completed

CompletedNCT04257201

Mushroom Ingestion Study

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
7 (actual)
Sponsor
Purdue University · Academic / Other
Sex
All
Age
30 Years – 69 Years
Healthy volunteers
Accepted

Summary

The investigators propose to determine the effect of consuming 0, 1 or 2 servings of white button (Agaricus bisporus; most popular, lower ergothioneine) or yellow oyster (Pleurotus citrinopileatus; higher ergothioneine) mushrooms on postprandial changes in plasma levels and urinary excretions of mushroom-specific compounds.

Detailed description

The investigators hypothesize that consuming different mushroom varieties will elicit distinct postprandial nutrimetabolomic profiles in the plasma and urine and that the amount of metabolites present will increase with the servings of mushrooms. Measuring ergothioneine in the plasma will provide a quantitative outcome to document the postprandial responses to consuming the test meals. The nutrimetabolomic related outcomes are exploratory and have not been documented in human research.

Conditions

Interventions

TypeNameDescription
OTHERYellow Oyster -- 84 gParticipants will consume the standardized test day salad plus 84 g (raw weight) mushrooms. Mushrooms will be cooked prior to being served
OTHERYellow Oyster -- 168 gParticipants will consume the standardized test day salad plus 168 g (raw weight) mushrooms. Mushrooms will be cooked prior to being served
OTHERWhite button -- 84 gParticipants will consume the standardized test day salad plus 84 g (raw weight) mushrooms. Mushrooms will be cooked prior to being served
OTHERWhite button -- 168 gParticipants will consume the standardized test day salad plus 168 g (raw weight) mushrooms. Mushrooms will be cooked prior to being served
OTHERControlParticipants will consume the standardized test day salad only

Timeline

Start date
2020-08-15
Primary completion
2021-05-21
Completion
2021-05-21
First posted
2020-02-05
Last updated
2024-02-16

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT04257201. Inclusion in this directory is not an endorsement.