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Trials / Terminated

TerminatedNCT00420407

Low Dose Vasopressin in Traumatic Shock

Prospective, Randomized, Double-Blind, Multi-Center Trial of Low Dose Vasopressin Versus Placebo in Traumatic Shock Resuscitation

Status
Terminated
Phase
EARLY_Phase 1
Study type
Interventional
Enrollment
81 (actual)
Sponsor
The University of Texas Health Science Center at San Antonio · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

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.

Conditions

Interventions

TypeNameDescription
DRUGnormal saline controlno vasopressin added to bolus or 5 hour continuous infusion
DRUGvasopressinvasopressin bolus 4 units followed by continuous infusion 2.4units/hr for 5 hours

Timeline

Start date
2007-02-01
Primary completion
2009-04-01
Completion
2011-02-01
First posted
2007-01-11
Last updated
2019-06-18
Results posted
2013-04-16

Locations

1 site across 1 country: United States

Regulatory

Source: ClinicalTrials.gov record NCT00420407. Inclusion in this directory is not an endorsement.

Low Dose Vasopressin in Traumatic Shock (NCT00420407) · Clinical Trials Directory