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Prospective, Randomized, Double-Blind, Multi-Center Trial of Low Dose Vasopressin Versus Placebo in Traumatic Shock Resuscitation
Hypothesis: We hypothesize that resuscitation regimens which minimize the total volume of resuscitation fluid, while restoring organ perfusion, will lead to lower morbidity and mortality in critically ill patients following trauma.
Age
18 - No limit years
Sex
ALL
Healthy Volunteers
No
University of Texas Health Science Center at San Antonio
San Antonio, Texas, United States
Start Date
February 1, 2007
Primary Completion Date
April 1, 2009
Completion Date
February 1, 2011
Last Updated
June 18, 2019
81
ACTUAL participants
normal saline control
DRUG
vasopressin
DRUG
Lead Sponsor
The University of Texas Health Science Center at San Antonio
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
View ClinicalTrials.gov Terms and ConditionsNCT05563103