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
| Type | Name | Description |
|---|---|---|
| DRUG | Low dose terlipressin | Terlipressin-2mg (low dose ) |
| DRUG | Noradrenaline | Noradrenaline at 7.5 mcg/min, maximum of 60mcg/min. stepped up every 15 min |
| DRUG | Noradrenaline | Noradrenaline- 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.