Influence of Antiviral Treatment to the Long-Term Prognosis of Patients With Chronic HBV Infection
This study is currently recruiting participants.
Verified October 2008 by Sun Yat-sen University
Sponsor:
Sun Yat-sen University
Information provided by:
Sun Yat-sen University
ClinicalTrials.gov Identifier:
NCT00810524
First received: December 1, 2008
Last updated: December 17, 2008
Last verified: October 2008
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Purpose
Influence of antiviral treatment to the long term prognosis of patients with chronic HBV infection. The aim of antiviral treatment for HBV is to reduce the long term severe complications. In this study, the investigators divided patients with chronic HBV infection into two groups, which start early antiviral treatment and conventional antiviral treatment respectively. All the patients will be followed for ten years. From this study, the investigators want to find out the optimal time for patients with chronic HBV infection to start antiviral treatment.
| Condition | Intervention | Phase |
|---|---|---|
|
Hepatitis B, Chronic |
Drug: lamivudine Drug: Telbivudine Drug: Enticavir Drug: Adefovir Dipivoxil Tablets |
Phase 4 |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Efficacy Study Intervention Model: Parallel Assignment Masking: Open Label Primary Purpose: Treatment |
| Official Title: | Influence of Antiviral Treatment to the Long-Term Prognosis of Patients With Chronic HBV Infection. |
Resource links provided by NLM:
Further study details as provided by Sun Yat-sen University:
Primary Outcome Measures:
- incidence rate of hepatic carcinoma [ Time Frame: 10 years after treatment ] [ Designated as safety issue: Yes ]
- incidence rate of liver cirrhosis [ Time Frame: 10 years after treatment ] [ Designated as safety issue: Yes ]
- incidence rate of fulminant hepatitis [ Time Frame: 10 years after treatment ] [ Designated as safety issue: Yes ]
| Estimated Enrollment: | 600 |
| Study Start Date: | January 2007 |
| Estimated Study Completion Date: | January 2017 |
| Estimated Primary Completion Date: | January 2017 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
Experimental: A
120 subjects (have family history of hepatic carcinoma or liver cirrhosis). Antiviral treatment are started when ALT is lower than 80u/L (early antiviral treatment).
|
Drug: lamivudine
100mg, P.O.,QD, duration: until HBeAg seroconversion for more than 2years.
Drug: Telbivudine
600mg, P.O.,QD, duration: until HBeAg seroconversion for more than 2years.
Drug: Enticavir
0.5mg, P.O.,QD, duration: until HBeAg seroconversion for more than 2 years.
Drug: Adefovir Dipivoxil Tablets
10mg, P.O.,QD, duration: until HBeAg seroconversion for more than 2years.
|
|
Active Comparator: B
120 subjects (have family history of hepatic carcinoma or liver cirrhosis). Antiviral treatment are started when ALT is higher than 80u/L (regular antiviral treatment).
|
Drug: lamivudine
100mg, P.O.,QD, duration: until HBeAg seroconversion for more than 2years.
Drug: Telbivudine
600mg, P.O.,QD, duration: until HBeAg seroconversion for more than 2years.
Drug: Enticavir
0.5mg, P.O.,QD, duration: until HBeAg seroconversion for more than 2 years.
Drug: Adefovir Dipivoxil Tablets
10mg, P.O.,QD, duration: until HBeAg seroconversion for more than 2years.
|
|
Experimental: C
180 subjects (have no family history of hepatic carcinoma or liver cirrhosis). Antiviral treatment are started when ALT is lower than 80u/L (early antiviral treatment).
|
Drug: lamivudine
100mg, P.O.,QD, duration: until HBeAg seroconversion for more than 2years.
Drug: Telbivudine
600mg, P.O.,QD, duration: until HBeAg seroconversion for more than 2years.
Drug: Enticavir
0.5mg, P.O.,QD, duration: until HBeAg seroconversion for more than 2 years.
Drug: Adefovir Dipivoxil Tablets
10mg, P.O.,QD, duration: until HBeAg seroconversion for more than 2years.
|
|
Active Comparator: D
180 subjects (have no family history of hepatic carcinoma or liver cirrhosis). Antiviral treatment are started when ALT is higher than 80u/L (regular antiviral treatment).
|
Drug: lamivudine
100mg, P.O.,QD, duration: until HBeAg seroconversion for more than 2years.
Drug: Telbivudine
600mg, P.O.,QD, duration: until HBeAg seroconversion for more than 2years.
Drug: Enticavir
0.5mg, P.O.,QD, duration: until HBeAg seroconversion for more than 2 years.
Drug: Adefovir Dipivoxil Tablets
10mg, P.O.,QD, duration: until HBeAg seroconversion for more than 2years.
|
Eligibility| Ages Eligible for Study: | 20 Years to 45 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Criteria
Inclusion Criteria:
- HBsAg positive for more than 6 months.
- HBeAg positive.
- HBV DNA over 10E5 copies/ml.
Exclusion Criteria:
- Previous antiviral treatment for HBV.
- Co infection of HIV, HCV, HEV, HAV, or HAV.
- Evidence of hepatic carcinoma.
- Evidence of autoimmune disease.
- Evidence of thyroid disease.
- History of mental sickness.
Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00810524
Contacts
| Contact: Gao zhiliang, M. D. | +862085252037 | zhanlianh@21cn.com |
| Contact: Huang zhanlian, M. D. | +8685252046 | zhanlianh@21cn.com |
Locations
| China, Guangdong | |
| Recruiting | |
| Guangzhou, Guangdong, China | |
| Contact: Gao zhiliang, M. D. +8685252037 | |
| Principal Investigator: gao zhiliang, doctor | |
| The Third Affiliated Hospital Of Sun Yat-sen University | Recruiting |
| Guangzhou, Guangdong, China | |
| Contact: Gao zhiliang, M. D. +862085252037 zhanlianh@21cm.com | |
Sponsors and Collaborators
Sun Yat-sen University
Investigators
| Study Director: | Gao zhiliang, M. D. | Third Affiliated Hospital, Sun Yat-Sen University |
More Information
No publications provided
| Responsible Party: | The Third Affliated Hospital of Sun Yat-sen University |
| ClinicalTrials.gov Identifier: | NCT00810524 History of Changes |
| Other Study ID Numbers: | SunYat-senU 5010 Hepatitis B |
| Study First Received: | December 1, 2008 |
| Last Updated: | December 17, 2008 |
| Health Authority: | United States: Institutional Review Board China: Food and Drug Administration |
Keywords provided by Sun Yat-sen University:
|
Chronic hepatitis B antiviral treatment long term prognosis |
Additional relevant MeSH terms:
|
Hepatitis Hepatitis A Hepatitis B Hepatitis B, Chronic Liver Diseases Digestive System Diseases Hepatitis, Viral, Human Virus Diseases Enterovirus Infections Picornaviridae Infections RNA Virus Infections Hepadnaviridae Infections DNA Virus Infections Hepatitis, Chronic |
Antiviral Agents Adefovir Adefovir dipivoxil Lamivudine Anti-Infective Agents Therapeutic Uses Pharmacologic Actions Reverse Transcriptase Inhibitors Nucleic Acid Synthesis Inhibitors Enzyme Inhibitors Molecular Mechanisms of Pharmacological Action Anti-Retroviral Agents Anti-HIV Agents |
ClinicalTrials.gov processed this record on May 23, 2013