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临床试验/NCT02297659
NCT02297659Unknown不适用

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

San Antonio Military Medical Center1 个研究点 分布在 1 个国家目标入组 312 人开始时间: 2014年8月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
入组人数
312
试验地点
1
主要终点
Number of participants who achieve primary fascial closure

研究概览

简要总结

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.

详细描述

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.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Triple (Participant, Care Provider, Investigator)

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

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

排除标准

  • •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.

研究组 & 干预措施

Crystalloid resuscitation

Active Comparator

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

干预措施: Primary Fascial Closure (Procedure)

Crystalloid resuscitation

Active Comparator

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

干预措施: wound vac dressing application (Device)

Hypertonic saline resuscitation

Active Comparator

Patients to receive 3% hypertonic saline resuscitation at a rate of 30cc/hr.

干预措施: Primary Fascial Closure (Procedure)

Hypertonic saline resuscitation

Active Comparator

Patients to receive 3% hypertonic saline resuscitation at a rate of 30cc/hr.

干预措施: wound vac dressing application (Device)

结局指标

主要结局

Number of participants who achieve primary fascial closure

时间窗: 2 weeks

Is there a higher rate of PFC among patients who undergo DCL and temporary abdominal closure when using HTS versus standard crystalloid resuscitation?

次要结局

  • number of anastomotic failure(90 days)
  • number of hospital free days(30 days)
  • number of abdominal wall hernias(90 days)
  • number of ventilator free days(30 days)
  • number of ICU free days(30 days)
  • number of enterocutaneous fistula(90 days)
  • number of intra abdominal abscess(90 days)

研究者

申办方类型
Fed
责任方
Principal Investigator
主要研究者

Valerie Sams

Acute Care Surgery Fellow

San Antonio Military Medical Center

研究点 (1)

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