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Effect of Terlipressin (drug) in liver disease.

Efficacy and Safety of Continuous Infusion of Terlipressin vs Bolus Terlipressin in ACLF Patients With Acute Esophageal Variceal Bleed -Pilot Study. - NIL

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/02/080135
Enrollment
60
Registered
2025-02-07
Start date
Unknown
Completion date
Unknown
Last updated
2025-03-03

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: Continous Infusion of Terlipressin: Administered as a continuous infusion at 4 mg per 24 hours. After 12 hours, if the hepatic venous pressure gradient (HVPG) does not show a reduction

Sponsors

Institute of Liver and Biliary Sciences
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Adult patients (age more than equals to 18 years) diagnosed with ACLF presenting with due to esophageal varices bleeding.

Exclusion criteria

Exclusion criteria: 1. History of coronary heart disease or ventricular arrhythmia, 2. Stroke or transient ischemic attack, 3. Bronchial asthma, 4. Epilepsy, 5. Pregnancy, 6. Rebleeding. 7. HCC 8. Gastric variceal bleed

Design outcomes

Primary

MeasureTime frame
HVPG responder at 12-24 hours in both armsTimepoint: 12-24 hours

Secondary

MeasureTime frame
Failure to control hemostasisTimepoint: 5 days;Terlipressin-related complications within 5 days i.e. safety of the drugTimepoint: 5 days;Number of blood transfusions at 5 daysTimepoint: 5 days;Rebleed within 42 day.Timepoint: 42 days;Incidence of post-bleed AKI within 5 days.Timepoint: 5 days;6 weeks mortality in both groupsTimepoint: 6 weeks

Countries

India

Contacts

Public ContactDr Vinod Arora

Institute of Liver and Biliary Sciences

VINOD_UCMS@yahoo.com01146300000

Outcome results

None listed

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