ClinConnect ClinConnect Logo
Search / Trial NCT03144713

Efficacy and Safety of Terlipressin With Albumin Versus Midodrine With Albumin Versus Albumin Alone in Prevention of Paracentesis Induced Circulatory Dysfunction in Cirrhosis

Launched by INSTITUTE OF LIVER AND BILIARY SCIENCES, INDIA · May 8, 2017

Trial Information

Current as of May 20, 2025

Completed

Keywords

ClinConnect Summary

No description provided

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • 1. Patients with cirrhosis who undergo Large volume paracentesis (\> 5L)
  • 2. Patients with age from 18-75 years
  • Exclusion Criteria:
  • 1. Renal failure ( Creatinine\>1.5mg/dl)
  • 2. Recent Gastrointestinal bleeding within 7 days
  • 3. Spontaneous bacterial Peritonitis
  • 4. Patients with Cardiovascular disease (Electrocardiogram, 2D Echo)
  • 5. Systemic arterial hypertension ( \>160/90mmhg) Presence of hepatocellular carcinoma or portal vein thrombosis, Budd chiari syndrome
  • 6. Patients with active untreated sepsis
  • 7. Pregnancy
  • 8. Patients with hepatic encephalopathy
  • 9. No use of drugs affecting systemic hemodynamic 3 days prior to enrollment
  • 10. Refusal to participate

About Institute Of Liver And Biliary Sciences, India

The Institute of Liver and Biliary Sciences (ILBS) in India is a premier research and healthcare institution dedicated to the advancement of knowledge and treatment in liver, biliary, and related diseases. As a clinical trial sponsor, ILBS is committed to conducting innovative and ethically-driven research to improve patient outcomes and enhance therapeutic options in hepatology. The institute fosters collaboration among multidisciplinary teams of clinicians, researchers, and healthcare professionals, ensuring rigorous scientific methodologies and adherence to regulatory standards. Through its focus on translational research, ILBS aims to bridge the gap between laboratory discoveries and clinical applications, ultimately contributing to the global understanding and management of liver diseases.

Locations

New Delhi, Delhi, India

Patients applied

0 patients applied

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

Similar Trials