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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT06040814
Other study ID # 202201561B0
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date December 1, 2022
Est. completion date November 30, 2025

Study information

Verified date December 2022
Source Chang Gung Memorial Hospital
Contact CHIEN-HAO HUANG, MD
Phone +886 9753 66128
Email q12248@cgmh.org.tw
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Through this plan, it will provide many benefits to patients with liver cirrhosis complicated with sarcopenia and/or hepatic encephalopathy, their family members, and the government in Taiwan: 1. To explore the changes of fecal microbiota before and after treatment such as resistance training rehabilitation in patients with liver cirrhosis complicated with sarcopenia and/or hepatic encephalopathy as a reference for future fecal microbiota transplantation; 2. To measure the changes of sarcopenia level before and after rehabilitation; 3. To measure the changes of hepatic encephalopathy level before and after rehabilitation. These study results will certainly bring updated diagnostic tool, latest treatment options, avoid serious sequelae and reduce medical expenditure.


Description:

Chronic liver disease is notorious as Taiwan's national disease and more than 4,000 patients died of liver cirrhosis each year in Taiwan. Hepatic encephalopathy (HE) manifests from minimal HE (MHE) to overt HE (OHE). The diagnosis of covert HE (CHE) requires psychometric tests or neurophysiological tools. However, psychometric testing for patients with CHE is often neglected in Taiwan. On the basis of the capability to detect all forms of HE, further investigation on the association of HE with fecal microbiota alterations is urgently needed. It is because HE is associated with dysregulation in the gut-liver-brain axis, which includes intestinal barrier dysfunction and gut microbial dysbiosis. However, despite current standard of care (SOC) therapy i.e., lactulose and rifaximin, there remains a subset of patients who continue to suffer recurrence, which leads to further cognitive impairment, sarcopenia and readmissions. There remain several factors that can influence the microbiota, such as demographics (geographic area, sex and diet), etiology, drugs, interventions, and finally the sampling compartment. These factors need to be controlled for and considered in the interpretation of future studies. The microbiome dynamic change during rehabilitation in cirrhotic patients with sarcopenia has never been studied and is worth exploring. Furthermore, from our previous study, the investigators have shown that one-year efficacy of rifaximin add-on to lactulose is superior to lactulose alone in patients with cirrhosis complicated with recurrent HE in Taiwan. The investigators also have preliminary data showing that rehabilitation could improve patient's sarcopenia. Further cohort validation is urgently required. Our innovative research purposes: 1. To explore the changes of fecal microbiota before and after treatment such as resistance training rehabilitation as a reference for future fecal microbiota transplantation; 2. To measure the changes of sarcopenia levels before and after rehabilitation


Recruitment information / eligibility

Status Recruiting
Enrollment 120
Est. completion date November 30, 2025
Est. primary completion date November 30, 2025
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 20 Years and older
Eligibility Inclusion Criteria: - Patients with liver cirrhosis Exclusion Criteria: - unstable vital sign such as shock, coma or intubation status - Non-curative hepatocellular carcinoma (cannot receive operation, radiofrequency ablation, liver transplantation,etc - Un-curative malignancies - Poor-controlled diabetes mellitus (HbA1C?8) - Active alcoholism (male alcohol ?40g/day, or ?140g/week; female ? 30g/day, or ?70g/week - Psychiatric comorbidities - Neurologic comorbidities like Alzheimer's, Parkinson's, stroke with neurological deficit - Unable to speak - Bed-ridden status - Post- Liver transplantation.

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Rehabilitation Training
12 week Rehabilitation Training course

Locations

Country Name City State
Taiwan Chang Gung Memorial Hospital Taoyuan

Sponsors (1)

Lead Sponsor Collaborator
Chang Gung Memorial Hospital

Country where clinical trial is conducted

Taiwan, 

Outcome

Type Measure Description Time frame Safety issue
Primary Handgrip Strength Handgrip strength is an assessment of muscle strength. The cutoff value of the handgrip is < 30 kg in men and < 20 kg in women. 6 months
Primary Short Physical Performance Battery (SPPB) Short Physical Performance Battery (SPPB) is an assessment of physical performance. The cut-off value of the Short Physical Performance Battery (SPPB) score for determining sarcopenia is = 9. 6 months
Primary Dual-energy X-ray absorptiometry (DEXA) Dual-energy X-ray absorptiometry (DXA) is the gold-standard technique in the analysis of body composition. The cut-off value of appendicular skeletal muscle mass (ASMI) score for determining sarcopenia is < 7.0 kg/m^2 in men and < 5.4 kg/m^2 in women. 6 months
Primary Mini-Mental Status Examination (MMSE) Mini-Mental State Examination (MMSE) is one of the most commonly used methods in the assessment of cognitive mental status. The cut-off value of Mini-Mental State Examination (MMSE) score is < 28. 6 months
Primary Psychometric Hepatic Encephalopathy Score (PHES) The psychometric hepatic encephalopathy score (PHES) is the gold standard for diagnosing minimal hepatic encephalopathy (MHE). The cut-off value of the Psychometric Hepatic Encephalopathy Score (PHES) for determining minimal hepatic encephalopathy (MHE) is = -4. 6 months
Primary Animal Naming Test (ANT) The animal naming test (ANT) is an easy tool for the assessment of hepatic encephalopathy (HE). The cut-off value of the Animal Naming Test (ANT) score for determining hepatic encephalopathy (HE) is = 19. 6 months
Primary Blood cytokine levels [IL-6] Serum IL-6 level (pg/ mL) 6 months
Primary Blood ammonia levels [NH3] Serum ammonia level (µg/dL) 6 months
Primary Electroencephalogram (EEG) Quantified EEG spectral analysis:
Grade 0: Mean dominant frequency (MDF)> 6.8 Hz and no theta nor delta wave Grade 1: MDF > 6.8Hz and theta wave relative power ?35% Grade 2: MDF= 6.8 Hz and delta wave relative power<49% Grade 3: MDF= 6.8 Hz and delta wave relative power?49%
6 months
Primary Fecal Microbiota Check fecal microbiota taxonomy profile and relative abundance changes. 6 months
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