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Impact of Midodrine Administration on the Clinical Outcome of Septic Shock Patients

Septic Shock Clinical Trial

Official title:
Impact of Midodrine Administration on the Clinical Outcome of Septic Shock Patients

Clinical Trial Summary

1. Assess the impact of midodrine administration on weaning of IV vasopressors

2. Assess the cost effectiveness of using midodrine in critically ill patients

Clinical Trial Description

A prospective randomized controlled clinical trial on total 60 critically ill patients admitted to critical care medicine department with indication to IV vasopressor due to septic shock on admission or during intensive care unit stay and they are randomly assigned to either of 2 groups as follows

1. Group 1(n=30):will receive IV vasopressor infusion only

2. Group 2(n=30):will receive midodrine in addition to IV vasopressor infusion ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03911817
Study type Interventional
Source Ain Shams University
Contact
Status Completed
Phase Phase 4
Start date November 15, 2017
Completion date July 30, 2019
View Details
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