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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03587467
Other study ID # 2018001
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date December 1, 2017
Est. completion date December 1, 2020

Study information

Verified date July 2018
Source Zhongshan Hospital Xiamen University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Hepatitis B Virus(HBV) infection is a common infectious disease affecting up to 2 billion people worldwide. Around 650 thousand people died of liver failure, cirrhosis and primary liver cancer caused by chronic hepatitis B every year. Age is the main factor affecting the chronicity of hepatitis B, while 90% and 25% to 30% of hepatitis b virus(HBV) infection in perinatal and infant period will develop into chronic infection respectively. Whereas the proportion in patients above 5 years old is only 5% to 10%. Intestinal microbiota plays an important role in maintaining nomal physiological function of the intestine and the immune function of the body. It has been found that the disorder of intestinal microbiota is associated with numerous intestinal and parenteral diseases. Recently, the relationship between immune response and intestinal microbiota has been claimed. In a previous study using IMT to treat HBeAg positive chronic hepatits B patients combined with antiviral theraopy, 80% of them has reached HBeAg clearance. Increasing evidence suggests that the gut microbiota has evolved as a new important player in the pathogenesis of hepatitis B virus-induced chronic liver disease. However, the composition and structure alteration of the gut microbiota associated with the stage and progression of HBV infection remains unknown. Hence, we proposed a trial to detected gut microbiota of chronic HBV infected patients high-throughput 16S rRNA gene sequencing to elucidate the microbial influence which contribute to the microbial shift of patient in different stage.


Recruitment information / eligibility

Status Recruiting
Enrollment 90
Est. completion date December 1, 2020
Est. primary completion date December 1, 2020
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group N/A and older
Eligibility Inclusion Criteria:

1. Alcohol free history or alcohol consumption <140g per week in male, <70g per week in female

2. smooth and soft stool like sausage or snake

3. Voluntary participate in this study

Exclusion Criteria:

1. Syptom of digestive system disorder such as hematochezia, constipation, Abdominal distention, abdominal pain, diarrhea and jaundice within 1 month

2. Abormal results of several tests including: fecal routine, fecal occult blood test

3. Be diagnosed as enteritis within 1 month

4. Chronic obstructive pulmonary disease, renal insufficiency and other systemic diseases.

5. Autoimmune disease

6. Chronic fatigue syndrome and neuropsychic disease

7. A history of antibiotics, microecological preparation, gastrointestinal motility medicine, laxative, weight loss drug, Glucose lowering, blood fat regulation, glucocorticoid or immunosuppressor treatment within 1 month

8. History of organic diseases in digestive system such as gastrointestinal polyposis, ulcers, malignancies, etc.

9. History of gastrointestinal surgery

Study Design


Intervention

Other:
collect fecal specimens
collect fresh fecal specimens of participants

Locations

Country Name City State
China Zhongshan Hospital Affiliated to Xiamen University Xiamen Fujian

Sponsors (1)

Lead Sponsor Collaborator
Zhongshan Hospital Xiamen University

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Gut microbiota detected gut microbiota of participants through high-throughput 16S rRNA gene sequencing to elucidate the microbial influence which contribute to the microbial shift of patient in different stage. 1day
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