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Clinical Trials/NCT03145168
NCT03145168
Completed
Not Applicable

High Versus Low Target Mean Arterial Pressure in Septic Shock in Critically Ill Cirrhotics -A Randomized Controlled Trial

Institute of Liver and Biliary Sciences, India1 site in 1 country150 target enrollmentSeptember 19, 2018
ConditionsCirrhosis

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Cirrhosis
Sponsor
Institute of Liver and Biliary Sciences, India
Enrollment
150
Locations
1
Primary Endpoint
Survival in both groups
Status
Completed
Last Updated
3 years ago

Overview

Brief Summary

Study Design:

  • A randomized controlled study.
  • The study will be conducted on patients admitted to Department of Hepatology from April 2017 to October 2017 at ILBS, New Delhi
  • Study group will comprise of patients critically ill cirrhotics with septic shock

All included patients would be randomised to low target MAP group (60-65mm Hg) or high target group (80-85 mm of Hg). Patients older than 18 years of age will be enrolled if they have septic shock that is refractory to fluid resuscitation and if they required vasopressors (norepinephrine or epinephrine or terlipressin) at a minimum infusion rate of 0.1 μg per kilogram per minute. Standard criteria will be considered to define refractoriness to fluids. The target MAP would be maintained for a max. of 5 days or until recovery or shock and or AKI. In the high-target group, a reduction in vasopressor doses to maintain a mean arterial pressure of 65 to 70 mm Hg will be done in case of any of the prespecified serious adverse events that could potentially be related to an increased rate of vasopressor infusion occurred. These events could be: clinically relevant bleeding (i.e., transfusion requirements of at least 2 units of packed red cells), myocardial infarction (defined as typical electrocardiographic changes, with a concomitant increase in troponin, and segmental echocardiographic hypokinesia or akinesia, with the infarction confirmed, when possible, by means of coronary angiography), major ventricular arrhythmia, poorly tolerated supraventricular arrhythmia, mesenteric ischemia, and distal-limb ischemia.

• Septic shock would be defined as clinical construct of sepsis with persisting hypotension requiring vasopressors to maintain MAP>=65 mm of Hg and having a serum lactate >2 mmol/L despite adequate volume resuscitation

Registry
clinicaltrials.gov
Start Date
September 19, 2018
End Date
March 18, 2021
Last Updated
3 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Critically ill cirrhotics with septic shock

Exclusion Criteria

  • Patients with age less than 18 years
  • Severe known cardiopulmonary disease (structural or valvular heart disease, coronary artery disease, COPD)
  • Pregnancy
  • Chronic kidney disease on hemodialysis
  • Extremely moribund patients with an expected life expectancy of less than 24 hours
  • Failure to give informed consent from family members.
  • Hemodynamic instability requiring very high dose of vasopressors

Outcomes

Primary Outcomes

Survival in both groups

Time Frame: 28 days

Secondary Outcomes

  • Incidence of intradialytic hypotension in patients undergoing Renal Replacement Therapy(3 months)
  • Reversal of shock in both groups(Day 5)
  • Duration of mechanical ventilation(3 months)
  • Acute Kidney Injury in both groups.(Day 5)
  • Duration of Intensive Care Unit /Hospital stay(3 months)

Study Sites (1)

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