Use of Hypertonic Saline After Damage Control Laparotomy to Improve Early Primary Fascial Closure
NCT ID: NCT02297659
Last Updated: 2015-12-15
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
NA
312 participants
INTERVENTIONAL
2014-08-31
2017-01-31
Brief Summary
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Detailed Description
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Research Questions:
1. Primary Objective: Is there a higher rate of PFC among patients who undergo DCL and temporary abdominal closure when using HTS versus standard crystalloid resuscitation?
2. Secondary Objectives: Does successful and faster PFC reduce ICU, ventilator and hospital days?
3. Does faster and more successful PFC result in lower morbidity to include enterocutaneous fistula (ECF), intra-abdominal abscess (IAA), abdominal wall hernia, and anastomotic failure?
DCL is a common procedure wounded warriors undergo due to blast and other blunt and penetrating mechanisms of injury. This results in a significant population of warriors at risk for all of the complications and comorbidities that accompany an open abdomen. Thus, finding ways to not only achieve PFC but also to decrease the time to PFC will reduce these unwanted events.
The protocol design is a multi-institutional, prospective, double blind, randomized controlled trial of patients who undergo DCL for abdominal trauma requiring temporary abdominal closure and return to operating room for definitive treatment. All participating facilities are Level I Trauma Centers. Currently, the standard of care for damage control resuscitation involves all intravenous fluid solutions utilized in this study; normal saline, Ringer's lactate, Plasmalyte, and 3% saline (HTS). However, the type of fluid is selected based on surgeon preference alone. Investigators will randomize patients to normal saline at a resuscitation rate of 30 cc/hr or to 3% saline (HTS) at a resuscitation rate of 30cc/hr which will be initiated upon arrival to the ICU.
Conditions
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Keywords
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Study Design
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RANDOMIZED
PARALLEL
PREVENTION
TRIPLE
Study Groups
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Crystalloid resuscitation
Patients to receive normal saline resuscitation at a rate of 30cc/hr.
Primary Fascial Closure
Abdominal wall closure following damage control laparotomy.
wound vac dressing application
temporary abdominal wall closure with this device after damage control laparotomy
Hypertonic saline resuscitation
Patients to receive 3% hypertonic saline resuscitation at a rate of 30cc/hr.
Primary Fascial Closure
Abdominal wall closure following damage control laparotomy.
wound vac dressing application
temporary abdominal wall closure with this device after damage control laparotomy
Interventions
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Primary Fascial Closure
Abdominal wall closure following damage control laparotomy.
wound vac dressing application
temporary abdominal wall closure with this device after damage control laparotomy
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* Male and female patients 18 years or older.
Exclusion Criteria
* Patients who have more than 1/3 loss of abdominal wall due to trauma.
* Patients with baseline serum sodium of \<120 mEq/L or \>155 mEq/L.
18 Years
ALL
No
Sponsors
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San Antonio Military Medical Center
FED
Responsible Party
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Valerie Sams
Acute Care Surgery Fellow
Locations
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San Antonio Military Medical Center
San Antonio, Texas, United States
Countries
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Facility Contacts
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Valerie G Sams, MD
Role: primary
Michelle F Buehner, MD
Role: backup
References
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Harvin JA, Mims MM, Duchesne JC, Cox CS Jr, Wade CE, Holcomb JB, Cotton BA. Chasing 100%: the use of hypertonic saline to improve early, primary fascial closure after damage control laparotomy. J Trauma Acute Care Surg. 2013 Feb;74(2):426-30; discussion 431-2. doi: 10.1097/TA.0b013e31827e2a96.
Other Identifiers
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397284-1
Identifier Type: -
Identifier Source: org_study_id