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Yellow Oyster -- 168 g for Healthy Eating

N/A
Waitlist Available
Led By Wayne Campbell, PhD
Research Sponsored by Purdue University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 5 hours
Awards & highlights

Study Summary

This trial will test the effect of consuming 0, 1 or 2 servings of white button or yellow oyster mushrooms on postprandial changes in plasma levels and urinary excretions of mushroom-specific compounds.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~5 hours
This trial's timeline: 3 weeks for screening, Varies for treatment, and 5 hours for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Change in plasma glucose
Change in plasma insulin
Plasma ergothioneine
+2 more

Trial Design

5Treatment groups
Experimental Treatment
Active Control
Group I: Yellow Oyster -- 84 gExperimental Treatment1 Intervention
Subjects will be randomized to consume a test day salad with 0 g, 84 g (yellow oyster or white button) or 168 g (yellow or white button) mushrooms. Mushrooms will be cooked prior to serving.
Group II: Yellow Oyster -- 168 gExperimental Treatment1 Intervention
Subjects will be randomized to consume a test day salad with 0 g, 84 g (yellow oyster or white button) or 168 g (yellow or white button) mushrooms. Mushrooms will be cooked prior to serving.
Group III: White button 168 gExperimental Treatment1 Intervention
Subjects will be randomized to consume a test day salad with 0 g, 84 g (yellow oyster or white button) or 168 g (yellow or white button) mushrooms. Mushrooms will be cooked prior to serving.
Group IV: White button -- 84 gExperimental Treatment1 Intervention
Subjects will be randomized to consume a test day salad with 0 g, 84 g (yellow oyster or white button) or 168 g (yellow or white button) mushrooms. Mushrooms will be cooked prior to serving.
Group V: Control -- no mushroomsActive Control1 Intervention
Subjects will be randomized to consume a test day salad with 0 g, 84 g (yellow oyster or white button) or 168 g (yellow or white button) mushrooms. Mushrooms will be cooked prior to serving.

Find a Location

Who is running the clinical trial?

Purdue UniversityLead Sponsor
224 Previous Clinical Trials
72,796 Total Patients Enrolled
Mushroom CouncilOTHER
5 Previous Clinical Trials
293 Total Patients Enrolled
Wayne Campbell, PhD4.8201 ReviewsPrincipal Investigator - Purdue University
Riley Hospital for Children, Indiana University Health, North Hospital
Medical School - Indiana University, Doctor of Medicine
Methodist Hospital (Residency)
4 Previous Clinical Trials
144 Total Patients Enrolled
5Patient Review
I was surprised by how much I enjoyed my experience. Dr. O'Brian was great. He was thorough and I could tell that he cared about me as a patient. I felt confident that I was in good hands.

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
Recent research and studies
clinicaltrials.govStudy
Mushroom Ingestion Study
Wayne Campbell 2020. "Mushroom Ingestion Study". ClinicalTrials.gov. https://clinicaltrials.gov/ct2/show/NCT04257201.
~1 spots leftby Apr 2025
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