Use of Hypertonic Saline After Damage Control Laparotomy to Improve Early Primary Fascial Closure

NCT ID: NCT02297659

Last Updated: 2015-12-15

Study Results

Results pending

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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Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

312 participants

Study Classification

INTERVENTIONAL

Study Start Date

2014-08-31

Study Completion Date

2017-01-31

Brief Summary

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Damage control laparotomy (DCL) has proven to be a successful means to improve survival in severely injured patients.1-5 However, the consequences of not being able to close the fascia after the initial operation due to significant resuscitation leading to bowel and retroperitoneal edema, abdominal compartment syndrome, and continued acidosis, coagulopathy and hypethermia6-7 has led to a new challenge. Delays in primary fascial closure (PFC) contributes to increased fluid losses and nutritional demands,8-9 abdominal wall hernias, enterocutaneous fistula, and intra-abdominal infections.10-13 Hypertonic saline (HTS) use after DCL has been suggested to reduce bowel edema and resuscitation volumes, thus allowing for a quicker time to closure.14 Investigators will randomize patients to receiving HTS or standard crystalloid solutions after DCL and compare the time to PFC, rate of successful closure, and rate of complications associated with an open abdomen. The current failure rate of PFC after DCL is approximately 25%. Investigators believe they can improve PFC rates using hypertonic saline.

Detailed Description

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The use of HTS after DCL may decrease the rate of failure to achieve PFC and reduce the number of complications associated with an open abdomen.

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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Open Abdomen After Damage Control Laparotomy

Keywords

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damage control resuscitation laparotomy

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

PREVENTION

Blinding Strategy

TRIPLE

Participants Caregivers Investigators

Study Groups

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Crystalloid resuscitation

Patients to receive normal saline resuscitation at a rate of 30cc/hr.

Group Type ACTIVE_COMPARATOR

Primary Fascial Closure

Intervention Type PROCEDURE

Abdominal wall closure following damage control laparotomy.

wound vac dressing application

Intervention Type DEVICE

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.

Group Type ACTIVE_COMPARATOR

Primary Fascial Closure

Intervention Type PROCEDURE

Abdominal wall closure following damage control laparotomy.

wound vac dressing application

Intervention Type DEVICE

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.

Intervention Type PROCEDURE

wound vac dressing application

temporary abdominal wall closure with this device after damage control laparotomy

Intervention Type DEVICE

Other Intervention Names

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AbThera woulnd vac (KCI)

Eligibility Criteria

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Inclusion Criteria

* All admissions of trauma patients who sustain trauma necessitating damage control laparotomy.
* Male and female patients 18 years or older.

Exclusion Criteria

* Children (\<18 years old), prisoners, or pregnant patients.
* 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.
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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San Antonio Military Medical Center

FED

Sponsor Role lead

Responsible Party

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Valerie Sams

Acute Care Surgery Fellow

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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San Antonio Military Medical Center

San Antonio, Texas, United States

Site Status RECRUITING

Countries

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United States

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.

Reference Type BACKGROUND
PMID: 23354234 (View on PubMed)

Other Identifiers

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397284-1

Identifier Type: -

Identifier Source: org_study_id