effect of dexmedetomidine on the outcome of septic shock patients
Phase 3
Recruiting
- Conditions
- Septic shock.Other shock
- Registration Number
- IRCT20100107003014N22
- Lead Sponsor
- Sari University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 66
Inclusion Criteria
Patients with septic shock
patients treated with norepinephrine or vasopressor
Patients over the age of 18 years
Exclusion Criteria
uncontrolled diabet melitus
patients with severe hepatic failure
hypovolemic patients
patients with a history of beta blocker use
patients with a history of COPD
patients with sick sinus syndrome
patients with heart block 2,3
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Clinical success. Timepoint: Every hour to 12 hours and then 7 days after intervention. Method of measurement: Data collecting form.
- Secondary Outcome Measures
Name Time Method