Microbiota, Sarcopenia, and Hepatic Encephalopathy Change in Cirrhotic Patients Before and After Rehabilitation

NCT ID: NCT06040814

Last Updated: 2023-09-18

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

RECRUITING

Clinical Phase

NA

Total Enrollment

120 participants

Study Classification

INTERVENTIONAL

Study Start Date

2022-12-01

Study Completion Date

2025-11-30

Brief Summary

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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.

Detailed Description

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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

Conditions

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Hepatic Encephalopathy

Study Design

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Allocation Method

NON_RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Rehabilitation Training

Rehabilitation Training is provided to patients with Liver Cirrhosis combined with sarcopenia.

Group Type EXPERIMENTAL

Rehabilitation Training

Intervention Type BEHAVIORAL

12 week Rehabilitation Training course

No-Rehabilitation Training

No extra training is provided to patients with Liver Cirrhosis combined with sarcopenia.

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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Rehabilitation Training

12 week Rehabilitation Training course

Intervention Type BEHAVIORAL

Eligibility Criteria

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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.
Minimum Eligible Age

20 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Chang Gung Memorial Hospital

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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CHIEN-HAO HUANG

Role: PRINCIPAL_INVESTIGATOR

Linkou Chang Gung Memorial Hospital, Taoyuan, Taiwan

Locations

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Chang Gung Memorial Hospital

Taoyuan District, , Taiwan

Site Status RECRUITING

Countries

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Taiwan

Central Contacts

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CHIEN-HAO HUANG, MD

Role: CONTACT

+886 9753 66128

Facility Contacts

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CHIEN-HUNG CHEN, MD

Role: primary

+886 9753 66128

Other Identifiers

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202201561B0

Identifier Type: -

Identifier Source: org_study_id

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