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

NCT ID: NCT05728918

Last Updated: 2024-08-09

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

25 participants

Study Classification

INTERVENTIONAL

Study Start Date

2023-03-01

Study Completion Date

2024-05-30

Brief Summary

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

Detailed Description

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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.

Conditions

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Fatigue Syndrome, Chronic Cold

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

PREVENTION

Blinding Strategy

DOUBLE

Participants Investigators

Study Groups

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Placebo

Placeo group

Group Type PLACEBO_COMPARATOR

Placebo

Intervention Type DIETARY_SUPPLEMENT

Placebo capsule, two capsules/day (600 mg/day) for 3 months

Treatment

Experimental group

Group Type EXPERIMENTAL

Antrodia cinnamomea mycelia

Intervention Type DIETARY_SUPPLEMENT

Antrodia cinnamomea mycelia capsule, two capsules/day (600 mg/day) for 3 months

Interventions

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Antrodia cinnamomea mycelia

Antrodia cinnamomea mycelia capsule, two capsules/day (600 mg/day) for 3 months

Intervention Type DIETARY_SUPPLEMENT

Placebo

Placebo capsule, two capsules/day (600 mg/day) for 3 months

Intervention Type DIETARY_SUPPLEMENT

Eligibility Criteria

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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
Minimum Eligible Age

50 Years

Maximum Eligible Age

75 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Greenyn Biotechnology Co., Ltd.

INDUSTRY

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Ming-Shun Wu, MD

Role: PRINCIPAL_INVESTIGATOR

WanFang Hospital

Locations

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WanFang Hospital

Taipei, , Taiwan

Site Status

Countries

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Taiwan

Other Identifiers

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A-111-091

Identifier Type: -

Identifier Source: org_study_id

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