Integrated Traditional Chinese and Clinical Medicine for Chronic Hepatitis B and Its Complication
Shandong Provincial Integrated Traditional Chinese and Clinical Medicine(Chronic Hepatitis B and Its Complication) Prevention and Treatment Project
1 other identifier
interventional
276
1 country
1
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for phase_3
Started Dec 2021
Shorter than P25 for phase_3
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
October 10, 2021
CompletedFirst Posted
Study publicly available on registry
November 19, 2021
CompletedStudy Start
First participant enrolled
December 1, 2021
CompletedPrimary Completion
Last participant's last visit for primary outcome
June 30, 2022
CompletedStudy Completion
Last participant's last visit for all outcomes
December 30, 2022
CompletedNovember 19, 2021
November 1, 2021
7 months
October 10, 2021
November 16, 2021
Conditions
Outcome Measures
Primary Outcomes (1)
The incidence of hepatic encephalopathy
The incidence of hepatic encephalopathy after 12 weeks of treatment.
12 weeks of treatment
Study Arms (4)
group 1
EXPERIMENTALtraditional chinese medicine 1 and traditional chinese medicine 2 simulant
group 2
EXPERIMENTALtraditional chinese medicine 1 simulant and traditional chinese medicine 2
group 3
EXPERIMENTALtraditional chinese medicine 1 and traditional chinese medicine 2
group 4
PLACEBO COMPARATORtraditional chinese medicine 1 simulant and traditional chinese medicine 2 simulant
Interventions
We use two traditional Chinese medicine prescriptions to intervene in patients after TIPS
Eligibility Criteria
You may qualify if:
- 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.
You may not qualify if:
- 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.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
he First Affiliated Hospital of Shandong First Medical University & Shandong Provincial Qianfoshan Hospital
Jinan, Shandong, 250010, China
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- phase 3
- Allocation
- RANDOMIZED
- Masking
- QUADRUPLE
- Who Masked
- PARTICIPANT, CARE PROVIDER, INVESTIGATOR, OUTCOMES ASSESSOR
- Purpose
- TREATMENT
- Intervention Model
- CROSSOVER
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Professor
Study Record Dates
First Submitted
October 10, 2021
First Posted
November 19, 2021
Study Start
December 1, 2021
Primary Completion
June 30, 2022
Study Completion
December 30, 2022
Last Updated
November 19, 2021
Record last verified: 2021-11