Chronic Hepatitis bNCT05483049
Prevalence of Significant Liver Fibrosis and Inflammation in Chronic HBV Infected Patients in Grey Zone
An observational study of Chronic Hepatitis b, run by Ruijin Hospital.
Trial summary
To explore whether normal alanine aminotransferase (ALT) is associated with liver injury in a cohort of hepatitis B virus (HBV) infected patients in grey zone Read more about this study
- Who is it for?
- Any age
- Conditions the study is for
- Chronic Hepatitis b
- How many people
- 600 participants
- Where
- No sites listed yet
- Study dates
- 1 Sep 2022to 31 Aug 2023
- Phase
- Observational
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages Any age
- All sexes
- No healthy volunteers
- Child, Adult, Older adult
Study population: An estimated 600 chronic HBV infected patients who underwent liver biopsy between Jan, 2008 and December, 2021 will be enrolled.
Who may be able to join
- Treatment naïve
- serum HBsAg positive for >6 months
- Grey zone 1: HBeAg (+), HBV DNA >20 but < 107IU/mL, ALT ≤40 U/L
- Grey zone 2: HBeAg (-), HBV DNA > 2000 IU/mL, ALT ≤40 U/L
Who cannot join
- Co-infection with HCV, HDV or HIV
- decompensated cirrhosis
- other chronic liver diseases
Trial locations and contacts
No sites are listed yet.
About this study
To explore whether normal alanine aminotransferase (ALT) is associated with liver injury in a cohort of hepatitis B virus (HBV) infected patients in grey zone
Read the detailed description
Hepatitis B is caused by HBV infection, which can progress to chronic HBV infection after 6 months. HBV infection is a global public health problem, which can affect liver function and even threaten life health. HBV infection is worldwide prevalent, but the infection rate varies greatly in different regions. According to World Health Organization (WHO), there are about 257 million chronic HBV infections worldwide. The western Pacific region and Africa are the most prevalent regions of HBV, with the adult infection rate of 6.2% and 6.1% respectively. Most of Asia is a medium-high epidemic area 1. In 2014, Center for Disease Control and Prevention (CDC) conducted a serological epidemiological survey on hepatitis B among the population aged 1-29 in China, and the results showed that the prevalence rate of HBsAg in the population aged 1-4, 5-14 and 15-29 was 0.32%, 0.94% and 4.38%, respectively. It is estimated that the prevalence of HBsAg in the general population of China is 5-6%, and there are about 70 million chronic HBV infections, among which there are about 20-30 million chronic hepatitis B (CHB) patients. Chronic HBV infection increases the risk of liver fibrosis and hepatocellular carcinoma (HCC). The annual incidence of cirrhosis is 2-10% in CHB patients without antiviral therapy, and the annual incidence of HCC in patients with cirrhosis is 3-6%2.
The China 2019 Prevention and Treatment Guidelines of Chronic Hepatitis B recommend that patients with positive HBV DNA and elevated ALT, and those above 30 years old with family history of liver cirrhosis or HCC should initiate antiviral treatment, after ruling out other potential causes. However, the guideline did not identify the specific reference value of upper limit of normal for ALT, neither with cut off value of HBV detection. In addition, there is no clear definition of 'family history'. So, the fuzzy boundaries in the HBV guidelines may cause confusion when providing treatment recommendations in clinical practice and the value of this study would contribute to solve this kind of problems.
In a recently published study this year, 432 CHB patients who had liver biopsy in Ruijin Hospital during 2011-2017 were reviewed. So based on this, In the present study, we estimated a sample size of 600.Chronic HBV infected patients from 4 sites who underwent liver biopsy between 2008 and 2020.12 will be enrolled.
Previous studies have shown that a high proportion of HBV-infected patients with normal ALT have significant liver injury, including significant inflammation or fibrosis, and even cirrhosis.
And studies also show that treatment naive patients with normal ALT, either HBeAg-positive or HBeAg-negative, have a higher risk of developing HCC and even death than those in immune-active patients who received antiviral treatment (AVT). Therefore, early identification of patients with normal ALT but with significant liver inflammation or fibrosis is crucial.
- Conditions
- Chronic Hepatitis b
- Medical subject headings
- Hepatitis B, Chronic
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
| Study group | Role | What they receive |
|---|---|---|
| grey zone 1 | HBeAg (+), HBV DNA >20 but < 10000000IU/mL, ALT ≤40 U/L | |
| grey zone 2 | HBeAg (-), HBV DNA > 2000 IU/mL, ALT ≤40 U/L |
What is being measured
The primary outcome is the main question the study is designed to answer.
Prevalence of significant liver fibrosis.
Prevalence of significant liver fibrosis (G≥2) in patients in all patients.
Measured: from Jan, 2008 to December, 2021
Prevalence of significant liver inflammation.
Prevalence of significant liver inflammation (S≥2) in patients in all patients.
Measured: from Jan, 2008 to December, 2021
Secondary outcomes (16)
Prevalence of significant liver fibrosis in different age group in grey zone 1.
Prevalence of significant liver fibrosis (G≥2) in different age group (10 years old per group) in patients in grey zones 1.
Measured: from Jan, 2008 to December, 2021
Prevalence of significant liver inflammation in different age group in grey zone 1.
Prevalence of significant liver inflammation (S≥2) in different age group (10 years old per group) in patients in grey zones 1.
Measured: from Jan, 2008 to December, 2021
Prevalence of significant liver fibrosis in different age group in grey zone 2.
Prevalence of significant liver fibrosis (G≥2) in different age group (10 years old per group) in patients in grey zones 2.
Measured: from Jan, 2008 to December, 2021
Prevalence of significant liver inflammation in different age group in grey zone 2.
Prevalence of significant liver inflammation (S≥2) in different age group (10 years old per group) in patients in grey zones 2.
Measured: from Jan, 2008 to December, 2021
Prevalence of significant liver fibrosis at different ALT level in grey zone 1.
Prevalence of significant liver fibrosis (G≥2)at different ALT level (low normal level 0-25 U/L for women and 0-35 U/L for men, high normal level 26-40 U/L for women and 36-40 U/L for men) in patients in grey zones 1.
Measured: from Jan, 2008 to December, 2021
Prevalence of significant liver inflammation at different ALT level in grey zone 1.
Prevalence of significant liver inflammation (S≥2) at different ALT level (low normal level 0-25 U/L for women and 0-35 U/L for men, high normal level 26-40 U/L for women and 36-40 U/L for men) in patients in grey zones 1.
Measured: from Jan, 2008 to December, 2021
Prevalence of significant liver fibrosis at different ALT level in grey zone 2.
Prevalence of significant liver fibrosis (G≥2)at different ALT level (low normal level 0-25 U/L for women and 0-35 U/L for men, high normal level 26-40 U/L for women and 36-40 U/L for men) in patients in grey zones 2.
Measured: from Jan, 2008 to December, 2021
Prevalence of significant liver inflammation at different ALT level in grey zone 2.
Prevalence of significant liver inflammation (S≥2) at different ALT level (low normal level 0-25 U/L for women and 0-35 U/L for men, high normal level 26-40 U/L for women and 36-40 U/L for men) in patients in grey zones 2.
Measured: from Jan, 2008 to December, 2021
Prevalence of significant liver fibrosis at different DNA level in grey zone 1.
Prevalence of significant liver fibrosis (G≥2) at different DNA level (log10 IU/mL per group) in patients in grey zones 1.
Measured: from Jan, 2008 to December, 2021
Prevalence of significant liver inflammation at different DNA level in grey zone 1.
Prevalence of significant liver inflammation (S≥2) at different DNA level (log10 IU/mL per group) in patients in grey zones 1.
Measured: from Jan, 2008 to December, 2021
Prevalence of significant liver fibrosis at different DNA level in grey zone 2.
Prevalence of significant liver fibrosis (G≥2) at different DNA level (log10 IU/mL per group) in patients in grey zones 2.
Measured: from Jan, 2008 to December, 2021
Prevalence of significant liver inflammation at different DNA level in grey zone 2.
Prevalence of significant liver inflammation (S≥2) at different DNA level (log10 IU/mL per group) in patients in grey zones 2.
Measured: from Jan, 2008 to December, 2021
Prevalence of significant liver fibrosis with different family history of HCC in grey zone 1.
Prevalence of significant liver fibrosis (G≥2) with different family history of HCC or liver cirrhosis (first degree relative, second and third degree relatives) in patients in grey zones 1.
Measured: from Jan, 2008 to December, 2021
Prevalence of significant liver inflammation with different family history of HCC in grey zone 1.
Prevalence of significant liver inflammation (S≥2) with different family history of HCC or liver cirrhosis (first degree relative, second and third degree relatives) in patients in grey zones 1.
Measured: from Jan, 2008 to December, 2021
Prevalence of significant liver fibrosis with different family history of HCC in grey zone 2.
Prevalence of significant liver fibrosis (G≥2) with different family history of HCC or liver cirrhosis (first degree relative, second and third degree relatives) in patients in grey zones 2.
Measured: from Jan, 2008 to December, 2021
Prevalence of significant liver inflammation with different family history of liver cirrhosis in grey zone 2.
Prevalence of significant liver inflammation (S≥2) with different family history of HCC or liver cirrhosis (first degree relative, second and third degree relatives) in patients in grey zones 2.
Measured: from Jan, 2008 to December, 2021
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted1 Aug 2022
- Study start1 Sep 2022 (estimated)
- Primary completion31 Mar 2023 (estimated)
- Study completion31 Aug 2023 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Chronic Hepatitis bStudies of the same condition, open and under way.
- More trials run by Ruijin HospitalThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Cohort
- Time perspective
- Retrospective
- Enrolment
- 600 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Ruijin Hospital
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, WANG HUI, Ruijin Hospital
- Investigators
- Hui Wang, Principal investigator, Ruijin Hospital
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT05483049
- Sponsor's protocol ID
- liver injury-grey zone
- Status last verified
- Aug 2022
- First submitted
- 29 Jul 2022
- Last updated
- 10 Aug 2022
- Results posted
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Study at a glance
From the registry record, last updated by the sponsor on 10 Aug 2022. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Prevalence of Significant Liver Fibrosis and Inflammation in Chronic HBV Infected Patients in Grey Zone
- ClinicalTrials.gov ID
- NCT05483049
- Acronym / sponsor ID
- liver injury-grey zone
- Conditions
- Chronic Hepatitis b
- Study type
- Observational
- Recruitment status
- Unknown status
- Enrolment
- 600 participants (estimated)
- Lead sponsor
- Ruijin HospitalUniversity, hospital or other
- Study start
- 1 Sep 2022 (estimated)
- Primary completion
- 31 Mar 2023 (estimated)
- Study completion
- 31 Aug 2023 (estimated)
- First posted
- 1 Aug 2022 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
To explore whether normal alanine aminotransferase (ALT) is associated with liver injury in a cohort of hepatitis B virus (HBV) infected patients in grey zone
Detailed description
Hepatitis B is caused by HBV infection, which can progress to chronic HBV infection after 6 months. HBV infection is a global public health problem, which can affect liver function and even threaten life health. HBV infection is worldwide prevalent, but the infection rate varies greatly in different regions. According to World Health Organization (WHO), there are about 257 million chronic HBV infections worldwide. The western Pacific region and Africa are the most prevalent regions of HBV, with the adult infection rate of 6.2% and 6.1% respectively. Most of Asia is a medium-high epidemic area 1. In 2014, Center for Disease Control and Prevention (CDC) conducted a serological epidemiological survey on hepatitis B among the population aged 1-29 in China, and the results showed that the prevalence rate of HBsAg in the population aged 1-4, 5-14 and 15-29 was 0.32%, 0.94% and 4.38%, respectively. It is estimated that the prevalence of HBsAg in the general population of China is 5-6%, and there are about 70 million chronic HBV infections, among which there are about 20-30 million chronic hepatitis B (CHB) patients. Chronic HBV infection increases the risk of liver fibrosis and hepatocellular carcinoma (HCC). The annual incidence of cirrhosis is 2-10% in CHB patients without antiviral therapy, and the annual incidence of HCC in patients with cirrhosis is 3-6%2.
The China 2019 Prevention and Treatment Guidelines of Chronic Hepatitis B recommend that patients with positive HBV DNA and elevated ALT, and those above 30 years old with family history of liver cirrhosis or HCC should initiate antiviral treatment, after ruling out other potential causes. However, the guideline did not identify the specific reference value of upper limit of normal for ALT, neither with cut off value of HBV detection. In addition, there is no clear definition of 'family history'. So, the fuzzy boundaries in the HBV guidelines may cause confusion when providing treatment recommendations in clinical practice and the value of this study would contribute to solve this kind of problems.
In a recently published study this year, 432 CHB patients who had liver biopsy in Ruijin Hospital during 2011-2017 were reviewed. So based on this, In the present study, we estimated a sample size of 600.Chronic HBV infected patients from 4 sites who underwent liver biopsy between 2008 and 2020.12 will be enrolled.
Previous studies have shown that a high proportion of HBV-infected patients with normal ALT have significant liver injury, including significant inflammation or fibrosis, and even cirrhosis.
And studies also show that treatment naive patients with normal ALT, either HBeAg-positive or HBeAg-negative, have a higher risk of developing HCC and even death than those in immune-active patients who received antiviral treatment (AVT). Therefore, early identification of patients with normal ALT but with significant liver inflammation or fibrosis is crucial.
Study design
- Observational model
- Cohort
- Time perspective
- Retrospective
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| grey zone 1 | – | –HBeAg (+), HBV DNA >20 but < 10000000IU/mL, ALT ≤40 U/L |
| grey zone 2 | – | –HBeAg (-), HBV DNA > 2000 IU/mL, ALT ≤40 U/L |
Who may qualify
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Child, Adult, Older adult
- Study population
- An estimated 600 chronic HBV infected patients who underwent liver biopsy between Jan, 2008 and December, 2021 will be enrolled.
Key inclusion criteria (4 listed)
- Treatment naïve
- serum HBsAg positive for >6 months
- Grey zone 1: HBeAg (+), HBV DNA >20 but < 107IU/mL, ALT ≤40 U/L
- Grey zone 2: HBeAg (-), HBV DNA > 2000 IU/mL, ALT ≤40 U/L
Key exclusion criteria (3 listed)
- Co-infection with HCV, HDV or HIV
- decompensated cirrhosis
- other chronic liver diseases
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Primary outcome
Prevalence of significant liver fibrosis.
Time frame: from Jan, 2008 to December, 2021
Prevalence of significant liver fibrosis (G≥2) in patients in all patients.
Prevalence of significant liver inflammation.
Time frame: from Jan, 2008 to December, 2021
Prevalence of significant liver inflammation (S≥2) in patients in all patients.
16 secondary outcomes
Prevalence of significant liver fibrosis in different age group in grey zone 1.
Time frame: from Jan, 2008 to December, 2021
Prevalence of significant liver inflammation in different age group in grey zone 1.
Time frame: from Jan, 2008 to December, 2021
Prevalence of significant liver fibrosis in different age group in grey zone 2.
Time frame: from Jan, 2008 to December, 2021
Prevalence of significant liver inflammation in different age group in grey zone 2.
Time frame: from Jan, 2008 to December, 2021
Prevalence of significant liver fibrosis at different ALT level in grey zone 1.
Time frame: from Jan, 2008 to December, 2021
Prevalence of significant liver inflammation at different ALT level in grey zone 1.
Time frame: from Jan, 2008 to December, 2021
Prevalence of significant liver fibrosis at different ALT level in grey zone 2.
Time frame: from Jan, 2008 to December, 2021
Prevalence of significant liver inflammation at different ALT level in grey zone 2.
Time frame: from Jan, 2008 to December, 2021
Prevalence of significant liver fibrosis at different DNA level in grey zone 1.
Time frame: from Jan, 2008 to December, 2021
Prevalence of significant liver inflammation at different DNA level in grey zone 1.
Time frame: from Jan, 2008 to December, 2021
Prevalence of significant liver fibrosis at different DNA level in grey zone 2.
Time frame: from Jan, 2008 to December, 2021
Prevalence of significant liver inflammation at different DNA level in grey zone 2.
Time frame: from Jan, 2008 to December, 2021
Prevalence of significant liver fibrosis with different family history of HCC in grey zone 1.
Time frame: from Jan, 2008 to December, 2021
Prevalence of significant liver inflammation with different family history of HCC in grey zone 1.
Time frame: from Jan, 2008 to December, 2021
Prevalence of significant liver fibrosis with different family history of HCC in grey zone 2.
Time frame: from Jan, 2008 to December, 2021
Prevalence of significant liver inflammation with different family history of liver cirrhosis in grey zone 2.
Time frame: from Jan, 2008 to December, 2021
Results and safety
Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 10 Aug 2022.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Hui Wang principal investigator
Ruijin Hospital
Questions about this trial
What is this clinical trial studying?
An observational study of Chronic Hepatitis b, run by Ruijin Hospital.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 4 inclusion and 3 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: status not confirmed, as of the sponsor's last update on 10 Aug 2022. Status can change between updates, so confirm with the study contact before making plans.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
Results are not available in the source record.
How can a doctor refer a patient or contact the research team?
Contact Mingyang Feng (+8619821371901, fengmingyang1@163.com), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Prevalence of significant liver fibrosis. (time frame: from Jan, 2008 to December, 2021). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 10 Aug 2022.