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Clinical Trial Summary

This study aimed to determine whether hypertonic saline solution is effective in the resuscitation of injured patients undergoing abdominal damage control surgery regarding early closure of the abdominal wall.


Clinical Trial Description

A double-blind, controlled, randomized clinical trial was conducted to determine the impact of an infusion of hypertonic saline 3% vs. isotonic saline 0.9% at a dose of 50 mL/hr for the first 72 hours in patients with abdominal trauma requiring damage control surgery regarding some clinically relevant outcomes. These outcomes were: The timing of abdominal cavity closure, fluids balance, abdominal hypertension, and abdominal compartment syndrome occurrence, organ dysfunction, and 28 days' mortality. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02542241
Study type Interventional
Source Fundacion Clinica Valle del Lili
Contact
Status Terminated
Phase Phase 4
Start date November 27, 2015
Completion date September 4, 2018

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