Integrated Traditional Chinese and Clinical Medicine for Chronic Hepatitis B and Its Complication

Sponsor
Qianfoshan Hospital (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05128305
Collaborator
(none)
276
1
4
12.9
21.3

Study Details

Study Description

Brief Summary

Hepatic encephalopathy is the most common complication after TIPS, and hepatic encephalopathy occurs in almost all portosystemic shunts. For patients with severe upper gastrointestinal bleeding or refractory ascites in the decompensated chronic hepatitis B, transjugular intrahepatic portosystemic shunt (TIPS) is a very effective treatment. However, due to the severe complications such as hepatic encephalopathy after TIPS, the clinical application of TIPS is limited. Literature studies have shown that the incidence of encephalopathy after TIPS is about 35%. TIPS reduces the portal vena blood flow into the liver by establishing a new channel. But at the same time, the toxic substances from the gastrointestinal tract and other organs do not enter the liver to detoxify, and are more likely to enter the brain, leading to hepatic encephalopathy.

Moreover, studies have found that the liver and the intestine originate from the same germ layer and are closely related to each other in anatomy and function. There are a large number of microorganisms living in the intestinal tract. Normally, the intestinal tract, as the first defense of the human body, can effectively prevent bacteria and their products from entering the bloodstream. In cirrhosis and portal hypertension, blood return disorder causes intestinal damage. A series of microbes and product endotoxins such as gram-negative bacteria will enter the blood through the injury, and the toxins in the peripheral blood will enter the brain and cause hepatic encephalopathy happened.

The research team's early treatment plan with integrated traditional Chinese and Western medicine proved that it greatly reduced the incidence of hepatic encephalopathy after TIPS. And improve the clinical symptoms and signs of patients with liver cirrhosis, and improve the quality of life and survival of patients.

Condition or Disease Intervention/Treatment Phase
  • Drug: traditional Chinese medicine1 and traditional Chinese medicine 2
Phase 3

Study Design

Study Type:
Interventional
Anticipated Enrollment :
276 participants
Allocation:
Randomized
Intervention Model:
Crossover Assignment
Masking:
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
Shandong Provincial Integrated Traditional Chinese and Clinical Medicine(Chronic Hepatitis B and Its Complication) Prevention and Treatment Project
Anticipated Study Start Date :
Dec 1, 2021
Anticipated Primary Completion Date :
Jun 30, 2022
Anticipated Study Completion Date :
Dec 30, 2022

Arms and Interventions

Arm Intervention/Treatment
Experimental: group 1

traditional chinese medicine 1 and traditional chinese medicine 2 simulant

Drug: traditional Chinese medicine1 and traditional Chinese medicine 2
We use two traditional Chinese medicine prescriptions to intervene in patients after TIPS
Other Names:
  • traditional Chinese medicine1 simulant and traditional Chinese medicine 2 simulant
  • Experimental: group 2

    traditional chinese medicine 1 simulant and traditional chinese medicine 2

    Drug: traditional Chinese medicine1 and traditional Chinese medicine 2
    We use two traditional Chinese medicine prescriptions to intervene in patients after TIPS
    Other Names:
  • traditional Chinese medicine1 simulant and traditional Chinese medicine 2 simulant
  • Experimental: group 3

    traditional chinese medicine 1 and traditional chinese medicine 2

    Drug: traditional Chinese medicine1 and traditional Chinese medicine 2
    We use two traditional Chinese medicine prescriptions to intervene in patients after TIPS
    Other Names:
  • traditional Chinese medicine1 simulant and traditional Chinese medicine 2 simulant
  • Placebo Comparator: group 4

    traditional chinese medicine 1 simulant and traditional chinese medicine 2 simulant

    Drug: traditional Chinese medicine1 and traditional Chinese medicine 2
    We use two traditional Chinese medicine prescriptions to intervene in patients after TIPS
    Other Names:
  • traditional Chinese medicine1 simulant and traditional Chinese medicine 2 simulant
  • Outcome Measures

    Primary Outcome Measures

    1. The incidence of hepatic encephalopathy [12 weeks of treatment]

      The incidence of hepatic encephalopathy after 12 weeks of treatment.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 65 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • TIPS treatment criteria in line with the 2017 edition of the "Expert Consensus on Transjugular Intrahepatic Portosystemic Shunt" were selected to include patients with hepatitis B cirrhosis and Child-pugh grade A and B after TIPS surgery.

    • Patients with liver cirrhosis, portal hypertension, bleeding from esophagus and gastric varices; refractory pleural and ascites due to liver cirrhosis; incomplete portal vein/localized thrombosis in liver cirrhosis or primary and secondary prevention of cirrhosis, portal hypertension, esophagus and gastric varices bleeding.

    Exclusion Criteria:
    • Severe blood coagulation disorder (PTA≤20%) or platelets lower than 30×109/L;

    • Child-pugh classification of liver function C;

    • Those with respiratory and circulatory dysfunction;

    • Those whose systemic or focal infections have not been effectively controlled;

    • Patients with moderate to severe malnutrition;

    • Extensive primary or metastatic liver malignant tumors;

    • Those who are highly allergic to the products and drugs used in the treatment process.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 he First Affiliated Hospital of Shandong First Medical University & Shandong Provincial Qianfoshan Hospital Jinan Shandong China 250010

    Sponsors and Collaborators

    • Qianfoshan Hospital

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Lili Cao, Professor, Qianfoshan Hospital
    ClinicalTrials.gov Identifier:
    NCT05128305
    Other Study ID Numbers:
    • CT-2020-1230
    First Posted:
    Nov 19, 2021
    Last Update Posted:
    Nov 19, 2021
    Last Verified:
    Nov 1, 2021
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Nov 19, 2021