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Clinical Trials/NCT05728918
NCT05728918CompletedNot Applicable

Effectiveness of Antrodia Cinnamomea Mycelia on Improving Immune Response in Subhealth People

Greenyn Biotechnology Co., Ltd.1 site in 1 country25 target enrollmentStarted: March 1, 2023Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
25
Locations
1
Primary Endpoint
Immune analysis

Study Overview

Brief Summary

This study aims to assess the effect of Antrodia cinnamomea mycelia on immune modulation in subhealth people.

Detailed Description

This study aims to assess the effect of Antrodia cinnamomea mycelia on immune modulation in subhealth people: a randomized, double-blind, placebo-controlled, and parallel clinical investigation.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Prevention
Masking
Double (Participant, Investigator)

Eligibility Criteria

Ages
50 Years to 75 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •Subjects are easy to feel fatigued
  • •Subjects have poor sleep quality

Exclusion Criteria

  • •Pregnant women or preparing for pregnancy.
  • •Lactating women.
  • •Women gave birth 6 months before the study.
  • •Poor kindy and livers funcitons
  • •Severe cardiovascular or other chronic diseases
  • •Alcohol abuser
  • •Using immune-associated supplements

Arms & Interventions

Placebo

Placebo Comparator

Placeo group

Intervention: Placebo (Dietary Supplement)

Treatment

Experimental

Experimental group

Intervention: Antrodia cinnamomea mycelia (Dietary Supplement)

Outcomes

Primary Outcomes

Immune analysis

Time Frame: Baseline up to 4 weeks

Changes in T cell markers of 29 participants will be analyzed between baseline and week 4.

Antibody analysis

Time Frame: Baseline up to 4 weeks

Changes in IgA levels of 29 participants will be analyzed between baseline and week 4.

Cytokine analysis

Time Frame: Baseline up to 4 weeks

Changes in IL-1beta levels of 29 participants will be analyzed between baseline and week 4.

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Industry
Responsible Party
Sponsor

Study Sites (1)

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