Discontinuation Order of Vasopressors in Septic Shock
Information source: Samsung Medical Center
ClinicalTrials.gov processed this data on August 23, 2015 Link to the current ClinicalTrials.gov record.
Condition(s) targeted: Septic Shock
Intervention: Vasopressin (Drug); Norepinephrine (Drug)
Phase: N/A
Status: Terminated
Sponsored by: Samsung Medical Center Official(s) and/or principal investigator(s): kyeongman Jeon, M.D., Ph.D., Principal Investigator, Affiliation: Samsung Medical Center
Summary
The purpose of this study is to evaluate the incidence of hypotension based on the
discontinuation order of norepinephrine and vasopressin in patients receiving concomitant
norepinephrine and vasopressin infusions for the treatment of septic shock.
Clinical Details
Official title: Incidence of Hypotension Based on the Discontinuation Order of Vasopressors in the Management of Septic Shock
Study design: Allocation: Randomized, Endpoint Classification: Safety Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Subject), Primary Purpose: Supportive Care
Primary outcome: Incidence of hypotension
Secondary outcome: Time of hypotensionVasopressor free day 28-day mortality ICU mortality In-hospital mortality
Detailed description:
There are little data regarding the discontinuation of vasopressors in patients with septic
shock. Therefore, the investigators intend to evaluate the incidence of hypotension based on
the discontinuation order of norepinephrine and vasopressin in patients receiving
concomitant norepinephrine and vasopressin infusions for the treatment of septic shock.
Eligibility
Minimum age: 20 Years.
Maximum age: N/A.
Gender(s): Both.
Criteria:
Inclusion Criteria:
- patients 20 years of age or older
- patients of receiving concomitant therapy with norepinephrine and vasopressin for
teh management of septic shock
- patients began to reduce the vasopressor
Exclusion Criteria:
- patients who expired or had care withdrawn while receiving norepinephrine and
vasopressin
- patients being transferred into the ICU from an outside facility or the operating
room
- patients who are suspected to have vasopressin deficiency (eg. HPA axis dysfunction,
empty sella)
- acute myocardial infarction or Congestive heart failure (NYHA functional
classification III or IV)
- acute mesenteric ischemia
- patients who were received other vasopressor except for norepinephrine or vasopressin
Locations and Contacts
Samsung Medical Center, Seoul 135-710, Korea, Republic of
Additional Information
Starting date: December 2011
Last updated: January 28, 2015
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