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OpenTrials
Completed

NCT Number: NCT00754156

ABRA Abdominal Closure System in Open Abdomen Management

For the last 20 to 30 years, damage control laparotomy and decompressive laparotomy have emerged as part of the armamentariums for treatment of complex abdominal trauma, abdominal compartment syndrome, and critically ill surgical patients with profound acidosis. While these advances have saved lives, they have also led to a dramatic increase in patients with open abdominal cavities. Various methods have been employed to offer protection to the viscera and at the same time, encourage gradual closure of the abdominal fascia. Some of the techniques have included the Bogota bag, vacuum pack described by Barker , Wittman patch , and the use of vacuum assisted fascia-closure, including the commercially available system offered by KCI. Overall, the abdominal closure rate is approximately 50% to 90% over an average of 10 days. Unfortunately, there has been no well-designed comparison study available. Some of the best results also require returning to the operating room every 3 to 5 days.

At the University of Kentucky Medical Center, a combination of the vacuum pack dressing described by Barker, the commercially available VAC system (V.A.C.; KCI International, San Antonio, TX) and vicryl mesh closure systems are used. The primary fascial closure rate is approximately 50%. It is not standard practice to take patients to the OR every 3-5 days routinely.

Recently, a new FDA listed system (ABRA by Canica) has been introduced using a progressive tension system as a novel approach to the management of open abdomen. ABRA provides a dynamic reduction of full thickness, severely retracted midline abdominal defects with the goal of maintaining or restoring the primary closure option. This subdermal method uses button anchors and elastomer to gradually pull the wound margins together. Tension can be set and adjusted according to the desired outcome; to stabilize a retracted wound, reduce the wound, close the wound or prevent wound dehiscence (Attachment 1: Company brochure). Currently there is only one published case report of the success of this device. We hope to be the first center to prospectively report a series of patients with open abdomen managed with the new ABRA system. In this study, this system will be used in combination with a standard therapy used in abdominal wound closure at the University of Kentucky Medical Center. This system is called the V.A.C system (V.A.C.; KCI International, San Antonio, Tx). This therapy provides active exudate management and containment, assists in reducing abdominal volume and adds structural stabilization to adipose tissue.

Although no highly powered study has been done to establish data on performance, individual experiences at several institutions have reached fascial closure rates of higher than 70% using the ABRA device. One institution in Las Vegas, Nevada is using the ABRA device in combination with the VAC system and has experienced 100% closure rate to date with 12 patients. The purpose of this study is to collect information about the ABRA system in combination with the VAC technique at the University of Kentucky Medical Center. It is our belief that using this system will improve the fascial closure rate and thereby produce less chance of hernia and reduce long periods of open abdominal wounds. The objective of the study is to evaluate a novel approach for closure of open abdomen utilizing the Canica ABRA system combined with the K.C.I. VAC System to KCI VAC System alone.

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Key information

Age range

18 year–70 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

University of Kentucky Medical Center

Lexington, Kentucky, 40536, United States

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • ages of 18 and 70
  • patients deemed not a candidate for primary fascial closure at the second laparotomy.

Exclusion criteria

  • High risk for imminent death, as determined by the attending surgeon and PI
  • Pre-existing large ventral hernia
  • Significant loss of abdominal wall fascia as a result of trauma or infection
  • Known Crohn's disease
  • Pregnancy

Treatment and study plan

ABRA Abdominal Closure System

Device

ABRA Abdominal Closure System

V.A.C. Therapy

Device

V.A.C. Therapy Alone

KCI AbThera

Device

KCI ABThera

Primary outcomes

  1. Primary Closure Rate

    Time frame: up to 12 months

    The rate in which the abdomen was closed the first time.

  2. Number of Trips to the Operating Room

    Time frame: 12 Months

  3. Operating Room Time Utilization

    Time frame: Duration of Hospital Stay less than 6 months

    The amount of time needed to manage the open abdomen inside the operating room.

Secondary outcomes

  1. Days to Closure

    Time frame: Duration of Hospital Stay less than 6 months

  2. ICU Days

    Time frame: Duration of hospital stay less than 6 months

  3. Hospital Days

    Time frame: Duration of Hospital Stay less than 6 months

  4. Blood Transfused

    Time frame: Duration of Hospital Stay less than 6 months

Sponsors and collaborators

Lead sponsor

Anna Rockich

Other

Registry information

Official study title

A Prospective, Controlled Evaluation of ABRA Abdominal Wall Closure System in Combination With V.A.C. Therapy Compared to V.A.C. Alone in the Management of Open Abdomen

Acronym: ABRA

Important dates

Study start
2008
Primary completion
2011
Study completion
2011
First posted
Sep 17, 2008
Registry last updated
Mar 3, 2017

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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