search
Back to results

A Clinical Evaluation on Traditional Chinese Medicine Diagnosis and Treatment Program Blocking and Reversing Hepatitis B-related Liver Fibrosis - a Randomized, Controlled, Double-blind, Multi-center Clinical Trial

Primary Purpose

Liver Fibrosis, Chronic Hepatitis B

Status
Unknown status
Phase
Phase 4
Locations
China
Study Type
Interventional
Intervention
Fufang Biejia Ruangan Tablet
Placebo
Sponsored by
Beijing 302 Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Liver Fibrosis

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

Inclusion criteria of chronic hepatitis B related liver fibrosis:

  1. Age from 18 to 65 years old, male or female;
  2. Consistent with the diagnosis criteria of chronic hepatitis B;
  3. liver fibrosis(liver biopsy) stage F ≥ 3 (Ishak), HBV DNA ≥ 104 copies / ml (or ≥ 2000 IU / ml) were;
  4. TCM syndrome type: blood stasis, blood deficiency with toxic heat retention;
  5. Not taking over nucleoside antiviral in one year, no drug treatment of liver fibrosis in six months;
  6. Signed informed consent.

Exclusion Criteria:

  1. liver fibrosis(Liver biopsy) stage F <3 (Ishak);
  2. Combined with other severe chronic hepatitis, cirrhosis, liver cancer and other severe or end-stage liver disease;
  3. Accompanied by uncontrollable heart, kidney, lung, endocrine, blood, metabolic and gastrointestinal serious primary disease; or mental illness;
  4. Pregnant or lactating women;
  5. Patients with allergic constitution or allergic to TCM used;
  6. Not be prescribed medication, poor compliance, incomplete data affecting the efficacy and safety of those judgments;
  7. Patients unsuitable for this trial in Researchers' consideration;
  8. Co-infection with other viral liver disease.

Sites / Locations

  • 302 Military Hospital of ChinaRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

Fufang Biejia Ruangan Tablet

placebo

Arm Description

Fufang Biejia Ruangan Tablet will be administered to all of subjects in this arm.

placebo of Fufang Biejia Ruangan Tablet

Outcomes

Primary Outcome Measures

Liver histological changes

Secondary Outcome Measures

Full Information

First Posted
October 16, 2013
Last Updated
August 14, 2015
Sponsor
Beijing 302 Hospital
search

1. Study Identification

Unique Protocol Identification Number
NCT01965418
Brief Title
A Clinical Evaluation on Traditional Chinese Medicine Diagnosis and Treatment Program Blocking and Reversing Hepatitis B-related Liver Fibrosis - a Randomized, Controlled, Double-blind, Multi-center Clinical Trial
Study Type
Interventional

2. Study Status

Record Verification Date
August 2015
Overall Recruitment Status
Unknown status
Study Start Date
September 2013 (undefined)
Primary Completion Date
December 2015 (Anticipated)
Study Completion Date
undefined (undefined)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Beijing 302 Hospital

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This research puts liver biopsy as the enrollment screening criteria and the primary efficacy assessment indicators. Patients at different developmental stages of hepatitis B related liver fibrosis are respectively diagnosed and treated by Traditional Chinese medicine to determine optional diagnosis and treatment plan of traditional Chinese medicine to screen the advantage-treated population and to establish a treatment program, which can save national medical resources, for clinical application of Traditional Chinese medicine Diagnosis and Treatment blocking and reversing hepatitis B-related liver fibrosis. The research can help to build automation pathological analysis and diagnosis systems and non-invasive clinical assessment criteria and models of liver fibrosis which can be applied in clinical. It can also help to realize electronic patient data collection and management, to establish patients management centre and follow-up database. Then it will help to improve clinical efficacy of being blocked and reversed chronic hepatitis B related liver fibrosis by Chinese medicine Diagnosis and Treatment program, to reduce the incidence of liver cirrhosis and hepatitis B-related mortality, to prolong patients' survival and improve patients' quality of life, to make clinical efficacy, which is about Traditional Chinese Medicine blocking and revering chronic hepatitis B-related liver fibrosis, increase by 15% or more .

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Liver Fibrosis, Chronic Hepatitis B

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
1000 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Fufang Biejia Ruangan Tablet
Arm Type
Active Comparator
Arm Description
Fufang Biejia Ruangan Tablet will be administered to all of subjects in this arm.
Arm Title
placebo
Arm Type
Placebo Comparator
Arm Description
placebo of Fufang Biejia Ruangan Tablet
Intervention Type
Drug
Intervention Name(s)
Fufang Biejia Ruangan Tablet
Intervention Type
Drug
Intervention Name(s)
Placebo
Primary Outcome Measure Information:
Title
Liver histological changes
Time Frame
before treatment and after 48 weeks twice

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Inclusion criteria of chronic hepatitis B related liver fibrosis: Age from 18 to 65 years old, male or female; Consistent with the diagnosis criteria of chronic hepatitis B; liver fibrosis(liver biopsy) stage F ≥ 3 (Ishak), HBV DNA ≥ 104 copies / ml (or ≥ 2000 IU / ml) were; TCM syndrome type: blood stasis, blood deficiency with toxic heat retention; Not taking over nucleoside antiviral in one year, no drug treatment of liver fibrosis in six months; Signed informed consent. Exclusion Criteria: liver fibrosis(Liver biopsy) stage F <3 (Ishak); Combined with other severe chronic hepatitis, cirrhosis, liver cancer and other severe or end-stage liver disease; Accompanied by uncontrollable heart, kidney, lung, endocrine, blood, metabolic and gastrointestinal serious primary disease; or mental illness; Pregnant or lactating women; Patients with allergic constitution or allergic to TCM used; Not be prescribed medication, poor compliance, incomplete data affecting the efficacy and safety of those judgments; Patients unsuitable for this trial in Researchers' consideration; Co-infection with other viral liver disease.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Yongping Yang, Master
Phone
0086-13601371542
Email
yongpingyang@hotmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Yongping Yang, Master
Organizational Affiliation
Beijing 302 Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
302 Military Hospital of China
City
Beijing
State/Province
Beijing
ZIP/Postal Code
100039
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Hongyan Li, MD
Phone
+8618600346925
Email
hongyanlitj@yahoo.com
First Name & Middle Initial & Last Name & Degree
Feng Yu, MBBS
Phone
+861066933461
Email
yfeng0530@163.com
First Name & Middle Initial & Last Name & Degree
Yongping Yang, MD
First Name & Middle Initial & Last Name & Degree
Hongyan Li, MD
First Name & Middle Initial & Last Name & Degree
Jianhui Qu, MD

12. IPD Sharing Statement

Citations:
PubMed Identifier
32437567
Citation
Rong G, Chen Y, Yu Z, Li Q, Bi J, Tan L, Xiang D, Shang Q, Lei C, Chen L, Hu X, Wang J, Liu H, Lu W, Chen Y, Dong Z, Bai W, Yoshida EM, Mendez-Sanchez N, Hu KQ, Qi X, Yang Y. Synergistic Effect of Biejia-Ruangan on Fibrosis Regression in Patients With Chronic Hepatitis B Treated With Entecavir: A Multicenter, Randomized, Double-Blind, Placebo-Controlled Trial. J Infect Dis. 2022 Mar 15;225(6):1091-1099. doi: 10.1093/infdis/jiaa266.
Results Reference
derived
PubMed Identifier
25381721
Citation
Qu J, Yu Z, Li Q, Chen Y, Xiang D, Tan L, Lei C, Bai W, Li H, Shang Q, Chen L, Hu X, Lu W, Li Z, Chen D, Wang X, Zhang C, Xiao G, Qi X, Chen J, Zhou L, Chen G, Li Y, Zeng Z, Rong G, Dong Z, Chen Y, Lou M, Wang C, Lu Y, Zhang C, Yang Y. Blocking and reversing hepatic fibrosis in patients with chronic hepatitis B treated by traditional Chinese medicine (tablets of biejia ruangan or RGT): study protocol for a randomized controlled trial. Trials. 2014 Nov 10;15:438. doi: 10.1186/1745-6215-15-438.
Results Reference
derived

Learn more about this trial

A Clinical Evaluation on Traditional Chinese Medicine Diagnosis and Treatment Program Blocking and Reversing Hepatitis B-related Liver Fibrosis - a Randomized, Controlled, Double-blind, Multi-center Clinical Trial

We'll reach out to this number within 24 hrs