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Use of non invasive methods in Liver Dieseae for predicting bleed

Comparative Efficacy of Various Non-invasive Methods in Assessing Response to Beta-blockers as Secondary Prophylaxis for Acute Variceal Bleed

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2022/01/039146
Enrollment
200
Registered
2022-01-05
Start date
Unknown
Completion date
Unknown
Last updated
2022-10-17

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

Conditions

Health Condition 1: K746- Other and unspecified cirrhosis ofliver

Interventions

Intervention1: NIL: NIL Control Intervention1: NIL: NIL

Sponsors

Institute of Liver and Biliary Sciences
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1) Clinical / radiological /histologic diagnosis of cirrhosis (Child A&B) 2) Age >18 years 3) Advanced compensated liver disease of different etiology(Viral,metabolic,alcoholic) Upper GI bleed 4) Valid consent 5) No history of NSBB use in last 6 weeks

Exclusion criteria

Exclusion criteria: 1) Age > 70 years 2) Portal vein thrombosis 3) Underlaying shunts 4) Spleen anteroposterior diameter 5) Non cirrhotic portal hypertension 6) Only PHG, Ectopic varices 7) Heart rate 8) Pregnancy 9) obese(BMI >30mm of Hg) 10) HIV 11) HCC / Other malignancy 12) Other Comorbidities: Chronic kidney disease [ CrCl 9) 13) AST/ALT >5 times 14) Drug allergies 15) ACLF 16) Narrow intercoastal space 17) Failure to give informed consent from family members. 18) Patient enrolled in other clinical study

Design outcomes

Primary

MeasureTime frame
Change in HVPG and its correlation with non-invasive methods.Timepoint: 6 weeks

Secondary

MeasureTime frame
AAR, APRI, FIB 4 index, CSPH risk score,fibrosis index, GPR, King score, Lok score are other non invasive testsTimepoint: 6 weeks;Assessment of severity of portal hypertension by non-invasive methodsTimepoint: 6 weeks;Comparison of hypersplenism (Splenic volume and area) and hematological parameters before and after treatmentTimepoint: 6 weeks;Correlation and Cut-off values for non-invasive methods in responders and non-responders in relation to HVPGTimepoint: 6 weeks;Diagnosis and response assessment by convolutional neural network- AI based modelTimepoint: 6 weeks;Prognostic implication of HVPG rebleed on EVL with beta-blockersTimepoint: 6 weeks

Countries

India

Contacts

Public ContactDr Shiv Kumar Sarin

Institute of Liver and Biliary Sciences

shivsarin@gmail.com01146300000

Outcome results

None listed

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