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This study is a Clinical trial to assess the efficacy of nutrition support therapy of patients with liver failure. Patients were randomized to one of 2 groups to receive different nutrition and energy support treatment.
Patients with liver failure (defined by APASL) induced by any precipitating factors were randomized to two groups; a treatment group and a control group. Participants in treatment group were provided with a standard hospital diet that provided 25-30 kcal/kg/day . Patients in control group receive diet guide
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| a treatment group | Active Comparator | All study participants were provided with a standard hospital diet that provided B25-30 kcal/kg/day |
|
| control group | No Intervention | All study participants were not intervened with diet |
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| standard hospital diet | Dietary Supplement | patients were provided standard hospital diet that provided 25-30 kcal/kg/day |
|
| Measure | Description | Time Frame |
|---|---|---|
| Mortality at 30 day | The percentage of death of liver failure patients at 4 weeks | 4 weeks |
| Measure | Description | Time Frame |
|---|---|---|
| liver transplant-free survival | survival rate on 4 weeks and 3 month | 3month |
| Laboratory variables on serum biochemistry markers | Laboratory variables on serum lever of glutamic-pyruvic transaminase/glutamic oxalacetic transaminase/total bilirubin/ cholinesterase will be combined to report liver function |
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Inclusion Criteria:
Exclusion Criteria:
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| 3month |
| Laboratory variables on fasting blood sugar | Laboratory variables on serum lever of fasting blood sugar | 3month |