Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
The investigators conduct a randomized, double-blind, placebo-controlled study to investigate the effects of Fermented Protaetia brevitarsis seulensis powder on Alcohol-induced Liver Disease in adults for 8 weeks.
Previous studies have indicated that Fermented Protaetia brevitarsis seulensis powder may have the ability to improve liver function in adults with alcohol-induced liver disease. Therefore, the investigators conduct a randomized, double-blind, placebo-controlled study to investigate the effects of Fermented Protaetia brevitarsis seulensis powder on liver function in adults with alcohol-induced liver disease; the safety of the compound are also evaluate. The Investigators examine gamma-glutamyl transferase, alanine aminotransferase, aspartate aminotransferase, and other metabolic parameters at baseline, as well as after 4 and 8 weeks of intervention. Sixty adults were administered either 4,000 mg of Fermented Protaetia brevitarsis seulensis powder or a placebo each day for 8 weeks.
Not provided
Not provided
Not provided
Not provided
Not provided
| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Fermented Protaetia brevitarsis seulensis powder group | Experimental | This group takes Fermented Protaetia brevitarsis seulensis powder for 8 weeks |
|
| Placebo group | Placebo Comparator | This group takes placebo for 8 weeks |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Fermented Protaetia brevitarsis seulensis powder group | Dietary Supplement | This group takes Fermented Protaetia brevitarsis seulensis powder for 8 weeks |
|
| Measure | Description | Time Frame |
|---|---|---|
| Concentration of Gamma-Glutamyl Transpeptidase | Gamma-Glutamyl Transpeptidase | 8 weeks |
| Measure | Description | Time Frame |
|---|---|---|
| Concentration of Aspartate aminotransferase | Aspartate aminotransferase | 8 weeks |
| Concentration of Alanine aminotransferase | Alanine aminotransferase |
Not provided
Inclusion Criteria:
Exclusion Criteria:
Not provided
Not provided
Not provided
Not provided
Not provided
| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Sang Yeoup Lee, Professor | Contact | 360-2860 | 055 | saylee@pnu.edu |
| Ye Le Lee | Contact | 360-2860 | 055 | yeri1230@gmail.com |
| Name | Affiliation | Role |
|---|---|---|
| Sang Yeoup Lee, Professor | Pusan National University Yangsan Hospital | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Pusan National University Yangsan Hospital | Recruiting | Pusan | Ami-dong | 602-739 | South Korea |
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
| ID | Term |
|---|---|
| D008108 | Liver Diseases, Alcoholic |
| ID | Term |
|---|---|
| D008107 | Liver Diseases |
| D004066 | Digestive System Diseases |
| D020751 | Alcohol-Induced Disorders |
| D019973 | Alcohol-Related Disorders |
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
| Placebo group | Dietary Supplement | This group takes placebo for 8 weeks |
|
| 8 weeks |
| Fatigue Severity Scale | Fatigue Severity Scale, minimum~maximum values (1~7), higher scores mean a worse outcome. | 8 weeks |
| D019966 | Substance-Related Disorders |
| D064419 | Chemically-Induced Disorders |