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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01962155
Other study ID # 2013ZX10002005
Secondary ID
Status Completed
Phase N/A
First received October 5, 2013
Last updated September 8, 2016
Start date August 2013
Est. completion date September 2016

Study information

Verified date September 2016
Source Peking University First Hospital
Contact n/a
Is FDA regulated No
Health authority China: Ministry of Health
Study type Observational [Patient Registry]

Clinical Trial Summary

The aim of our prospective study is to construct and validate a non-invasive model consisting biochemical markers, FibroScan, and radiological parameters for evaluating liver fibrosis caused by hepatitis B virus in mainland China.


Description:

Up to Oct, 2015,total of 1800 patients with chronic HBV infection were enrolled. Paired blood and liver biopsy samples were collected. Blood samples stored at -80 degree Celsius. Liver biopsy samples were judged by three pathology experts.


Recruitment information / eligibility

Status Completed
Enrollment 1841
Est. completion date September 2016
Est. primary completion date December 2015
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria:

1. HBsAg positive for at least 6 months

2. agree to have liver biopsy

3. Male or female aged 18 to 65 years old

Exclusion Criteria:

1. Patients with alcoholic liver disease, autoimmune liver disease, heretic liver disease, drug induced liver disease,nonalcoholic liver disease or other chronic liver disease

2. platelet count < 80000/L

3. prothrombin activity = 60%

4. patients with any disease or condition which the investigator or treating physician feels would interfere with the trial or the safety of the subject

Study Design

Observational Model: Cohort, Time Perspective: Prospective


Locations

Country Name City State
China Peking University First Hospital Bei Jing Beijing
China 302 Military Hospital of China Beijing Beijing
China Beijing Ditan Hospital Beijing Beijing
China Beijing Youan Hospital, Capital Medical University Beijing
China China-Japan Friendship Hospital Beijing
China The 305 Hospital of People's Liberation Army Beijing
China The Second Xiangya Hospital of Central South Hospital Changsha Hunan
China West China Hospital, Sichuan University Chengdu
China Southwest Hospital, Third Military Medical University Chongqing Chongqing
China The Second Affiliated Hospital of Chongqing Medical University Chongqing Chongqing
China Dalian the Sixth People's Hospital Dalian Liaoning
China Guangzhou Eighth People's Hospital Guangzhou Guangdong
China The Third Affiliated Hospital of Sun Yat-sen University Guangzhou Guangdong
China Zhejiang First Hospital Hang Zhou Zhejiang
China The First Affiliated Hospital of Anhui Medical University Hefei Anhui
China 81 Military Hospital of China Nanjing Jiangsu
China The First Affiliated Hospital with Nanjing Medical University Nanjing Jiangsu
China The Second Hospital of Nanjing Nanjing Jiangsu
China The People's Hospital of Guangxi Zhuang Autonomous Region Nanning Guangxi
China The Third People's Hospital of Qinhuangdao Qinhuangdao Hebei
China Shanghai Public Health Clinical Center Shanghai
China Shanghai Ruijin Hospital Shanghai
China The Sixth People's Hospital of Shenyang Shenyang Liaoning
China The Third people's Hospital of Shenzhen Shenzhen Guangdong
China Shan Xi Medical University Taiyuan Shanxi
China Renmin Hospital of Wuhan University Wuhan Hubei
China Tongji Hospital of Tongji Medical College, Huazhong University of Science and Technology Wuhan Hubei
China The Third Affiliated Hospital of Xinxiang Medical University Xinxiang Henan
China Yantai City Hospital for Infectious Diseases Yantai Shandong
China Henan Provincial People's Hospital Zhengzhou Henan

Sponsors (1)

Lead Sponsor Collaborator
Peking University First Hospital

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary determine whether a non-invasive test or a combination of non invasive tests may be used to accurately evaluate liver fibrosis in patients with chronic hepatitis B singular evaluation at the time of liver biopsy No
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