Skip to content

Study for Effect and Mechanism of treating acute on chronic liver failur by Smilax glabra compound

Study for Effect and Mechanism of treating acute on chronic liver failur by Smilax glabra compound

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800020063
Enrollment
Unknown
Registered
2018-12-12
Start date
2019-01-01
Completion date
Unknown
Last updated
2018-12-18

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

Conditions

liver failur

Interventions

experimental group:Oral Compound of rhizoma smilacis glabra
Control group:Placebo

Sponsors

Ningbo 2nd Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18 to 65 years old men and women; 2. Previous diagnosis of chronic hepatitis B or post-hepatitis B cirrhosis; 3. TCM syndrome differentiation accords with: damp-heat yellowing, accumulation of epidemic toxins; manifestations: limb distress, poor acceptance, fatigue, lack of breath and laziness, head weight, abdominal distension, thick tongue coating, greasy tongue coating, pulse slippery; 4. At the same time, the diagnosis conforms to the performance criteria of HBV-ACLF syndrome: (1) Jaundice deepened rapidly, serum total bilirubin was 10 times higher than the upper limit of normal value or increased by more than 17.1 micromol/L per day; (2) Prothrombin activity (PTA) is less than 40% or INR is more than 1.5; (3) MELD-Na score < 30; 5. Compliance is good and follow-up principle can be observed.

Exclusion criteria

Exclusion criteria: 1. Complicated with severe infection (pulmonary and abdominal infection); 2. Complicated with renal impairment, creatinine value (>1.5 mg/dL) (133 umol/dL); 3. Hepatic encephalopathy grade 2 or above (West-Haven classification standard); 4. Liver malignant tumors; 5. Patients with HAV, HCV, HDV and HIV infection; 6. Alcoholic liver disease, autoimmune liver disease and hereditary metabolic liver disease; 7. Pregnant women and lactating women; 8. Those who suffer from other serious diseases affect the survival time of the patients; 9. Patients with other serious diseases affect follow-up compliance; 10. Subjects participating in other clinical studies.

Design outcomes

Primary

MeasureTime frame
the average 24-week survival time of HBV-ACLF;

Countries

China

Contacts

Public ContactQinzhi Deng

Ningbo 2nd Hospital

dqznbey@126.com+86 13957874855

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026