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Recruiting NCT05725044

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

Conditions: Fatigue

Sex: All
Ages: 30 Years – 64 Years
Healthy volunteers: 1
Phase: NA
Enrollment: 88
Sponsor: Amorepacific Corporation

Location: Korea, Republic of

Summary

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

Eligibility Criteria

Inclusion Criteria:- CIS > 76 pointsExclusion Criteria:A person who feels tired due to surgical operation within 6 months.drug/alcoholic hepatitis, cirrhosis, and fatty liveranorexia or bulimiaa person on night duty, shift work, or heavy redundancyA person who is unable to perform an exercise load testA person who implements professional exercise therapy, counseling therapy, etc. within two months of visit 1 to improve chronic fatigue.A person who has used drugs, functional foods, health supplements, and herbal medicines within two months of visiting to improve chronic fatigue.A person who continues to exercise regularly within three months of visitingImmunosuppressants, sleep-inducing drugs, antidepressants, sleeping pills, and antihistamines

Interested in this study? View the official listing for contact and enrollment details.

View on ClinicalTrials.gov

Source: ClinicalTrials.gov (NCT05725044). StuddyBuddy aggregates publicly available trial information.