Clinical Trials Directory

Trials / Completed

CompletedNCT02468063

To Assess the Efficacy of Early Introduction of a Combination of Low Dose Vasopressin Analogue in Addition to Noradrenaline as a Vasopressor in Patients of Cirrhosis With Septic Shock

A Prospective Study to Assess the Efficacy of Early Introduction of a Combination of Low Dose Vasopressin Analogue in Addition to Noradrenaline as a Vasopressor in Patients of Cirrhosis With Septic Shock

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
184 (actual)
Sponsor
Institute of Liver and Biliary Sciences, India · Academic / Other
Sex
All
Age
18 Years – 70 Years
Healthy volunteers
Not accepted

Summary

The consecutive patients admitted to Intensive care unit of Hepatology department of ILBS and full filling all the eligibility criteria will be enrolled in 1:1 ration by the process of randomization.- The study is an open level study. The investigators will strictly follow the randomization table to give therapy as per the intervention arm. * Intervention:-the therapeutic intervention is vasopressor i.e. noradrenaline alone and terlipressin along with noradrenaline to maintain the MAP \>65mm Hg. * Intervention arm * Arm (A) - Noradrenaline * Arm (B) - Noradrenaline + low dose terlipressin

Conditions

Interventions

TypeNameDescription
DRUGLow dose terlipressinTerlipressin-2mg (low dose )
DRUGNoradrenalineNoradrenaline at 7.5 mcg/min, maximum of 60mcg/min. stepped up every 15 min
DRUGNoradrenalineNoradrenaline- 3.75 mcg/min to 30 mcg/min. stepped up every 15 min

Timeline

Start date
2015-05-01
Primary completion
2017-05-31
Completion
2017-05-31
First posted
2015-06-10
Last updated
2017-11-06

Locations

1 site across 1 country: India

Source: ClinicalTrials.gov record NCT02468063. Inclusion in this directory is not an endorsement.