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Study on the new strategy and key techniques for accurate prevention and treatment of nonalcoholic steatohepatitis based on intestinal target bacteria

Study on the new strategy and key techniques for accurate prevention and treatment of nonalcoholic steatohepatitis based on intestinal target bacteria

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1800016178
Enrollment
Unknown
Registered
2018-05-17
Start date
2018-05-01
Completion date
Unknown
Last updated
2019-10-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

nonalcoholic steatohepatitis

Interventions

Case series:Diet

Sponsors

Affiliated Hospital of Hangzhou Normal University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Male and female aged 18 to 75 years old; 2. BMI 1.5ULN or liver biopsy confirmed as NASH; 4. Patients taking antihypertensive medications require blood pressure to be stable with stable daily doses of antihypertensive medication within 2 months prior to enrollment. <140/90mmHg); During the clinical trial, patients can continue to take antihypertensive drugs; 5. Patients taking statin/fibrate lipid-lowering drugs, requiring a stable daily dose within 3 months before enrollment, in clinical During the trial, patients can continue to take lipid-lowering drugs; 6. did not receive the following drugs within 3 months before enrollment (metformin, thiazolidinedione hypoglycaemic agents, DPP-4 inhibitors, GLP-1, SGLT2 inhibitors, polyene phosphatidylcholine, glycyrrhizic acid preparation, bicyclol, reduced glutathione, S-adenosylmethionine, silymarine, OCA/UDCA, betaine, fish oil, phosphodiesterase inhibitor, Kyrgyzstan Non-rozzies, probiotics and long-term antibiotics for more than 1 week); 7. Understand this study and signed informed consent.

Exclusion criteria

Exclusion criteria: 1. in the past 5 years, alcohol and/or drug abuse and dependence; 2. female average daily alcohol intake >10g/days, male average daily alcohol intake >20g/days; 3. combined with other acute and chronic active liver disease (viral hepatitis, hereditary scarlet disease, hepatolenticular degeneration, ?-resistance to trypsin deficiency, alcoholic liver disease, drug-related liver disease); 4. cirrhosis patients; 5. The Heart function is not complete, the heart function grade is 2, 3 or 4; 6. with heart pacemaker patients; 7. uncontrolled hypertension; 8. renal insufficiency, blood creatinine > normal upper limit; 9. pregnant or lactating women; 10. female early Pregnancy screening test positive, or the observation period does not want to contraceptive person; 11. The combination of HIV infection; 12. cannot accept MRI examination; 13. Long-term use of antibiotics (> 1 weeks); 14. uncontrolled hypothyroidism (upper limit of normal tsh>2 times); 15. Other researchers do not think that the completion of clinical trials.

Design outcomes

Primary

MeasureTime frame
glutamic-pyruvic transaminase;glutamic oxalacetic transaminase;gamma-glutamyltransferase;alkaline phosphatase;MRI-PDFF;

Countries

China

Contacts

Public ContactJunping Shi

Affiliated Hospital of Hangzhou Normal University

13957121199@vip.126.com+86 13957121199

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 16, 2026