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
| Type | Name | Description |
|---|---|---|
| DIETARY_SUPPLEMENT | Ginsengberry concentrate | Ginsengberry concentrate |
| DIETARY_SUPPLEMENT | Placebo | Placebo |
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.