Clinical Trials Directory

Trials / Completed

CompletedNCT05725044

Clinical Trial to Evaluate of Efficacy and Safety of Ginsengberry Concentrate on Fatigue.

Evaluation of Efficacy and Safety of Ginsengberry Concentrate on Fatigue: Randomized, Double-blind, and Placebo-controlled Trial.

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
88 (actual)
Sponsor
Amorepacific Corporation · Industry
Sex
All
Age
30 Years – 64 Years
Healthy volunteers
Accepted

Summary

The investigators conduct a 8-week, randomized, double-blind, placebo-controlled study to evaluate the efficacy and safety of ginsengberry concentrate on fatigue.

Detailed description

Previous studies have indicated that ginseng root may have the ability to improve fatigue. Therefore, the investigators conduct a randomized, double-blind, placebo-controlled study to investigate the effects of ginsengberry concentrate on Improvement of Fatigue in adults; the safety of the compound are also evaluate. The Investigators examine FSS(fatigue severity scale), CIS, lactate, Ammonia, Exercise test at baseline, as well as after 4 and 8 weeks of intervention. 88 adults were administered either ginsengberry concentrate or a placebo each day for 8 weeks.

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTGinsengberry concentrateGinsengberry concentrate
DIETARY_SUPPLEMENTPlaceboPlacebo

Timeline

Start date
2021-12-13
Primary completion
2023-03-03
Completion
2023-05-03
First posted
2023-02-13
Last updated
2023-05-26

Locations

1 site across 1 country: South Korea

Source: ClinicalTrials.gov record NCT05725044. Inclusion in this directory is not an endorsement.