A Study on Nutrition Support Therapy of Patients With Liver Failure

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

100 participants

Study Classification

INTERVENTIONAL

Study Start Date

2019-05-10

Study Completion Date

2022-06-01

Brief Summary

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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.

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Detailed Description

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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

Conditions

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Nutrition

Study Design

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Allocation Method

NON_RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

SUPPORTIVE_CARE

Blinding Strategy

NONE

Study Groups

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a treatment group

All study participants were provided with a standard hospital diet that provided B25-30 kcal/kg/day

Group Type ACTIVE_COMPARATOR

standard hospital diet

Intervention Type DIETARY_SUPPLEMENT

patients were provided standard hospital diet that provided 25-30 kcal/kg/day

control group

All study participants were not intervened with diet

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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standard hospital diet

patients were provided standard hospital diet that provided 25-30 kcal/kg/day

Intervention Type DIETARY_SUPPLEMENT

Eligibility Criteria

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Inclusion Criteria

1. Male and female patients from 18 to 65 years of age;

Exclusion Criteria

1. Surgery with in 4 weeks
2. three degree hepatoencephalopathy
3. malignant tumors
4. cardiac failure or respiratory failure
5. liver transplantation within observing period -

Minimum Eligible Age

18 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No