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Prevention of Incisional Hernia After Elective Open Abdominal Aortic Aneurysm (AAA) Repair

Primary Purpose

Abdominal Aortic Aneurysm

Status
Terminated
Phase
Not Applicable
Locations
Switzerland
Study Type
Interventional
Intervention
Ultrapro® Mesh implantation
Standard wound closure
Sponsored by
Cantonal Hospital of St. Gallen
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Abdominal Aortic Aneurysm focused on measuring Abdominal aortic aneurysm, Abdominal hernia

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patient scheduled for elective or early elective open repair of aortic aneurysm

Exclusion Criteria:

  • Emergency surgery
  • EVAR (endovascular procedure)
  • Patients with previous midline laparotomy
  • Patients with in situ abdominal mesh after previous hernia repair
  • Patients with large diastasis of abdominal wall
  • Allergy to penicillin
  • Women before menopause (mesh can interfere with potential future pregnancies)

Sites / Locations

  • Kantonsspital St. Gallen, Department of Surgery

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Mesh implantation

Standard wound closure without a mesh

Arm Description

Ultrapro® Mesh implantation

Standard wound closure

Outcomes

Primary Outcome Measures

Incidence of incisional hernia

Secondary Outcome Measures

Rate of postoperative complications
operation time
Rate of adverse events
Adverse events related to mesh implantation

Full Information

First Posted
February 20, 2008
Last Updated
September 15, 2023
Sponsor
Cantonal Hospital of St. Gallen
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1. Study Identification

Unique Protocol Identification Number
NCT01189708
Brief Title
Prevention of Incisional Hernia After Elective Open Abdominal Aortic Aneurysm (AAA) Repair
Official Title
Prevention of Incisional Hernia After Elective Open Abdominal Aortic Aneurysm Repair
Study Type
Interventional

2. Study Status

Record Verification Date
September 2023
Overall Recruitment Status
Terminated
Why Stopped
Treatment without success, low enrollment, one serious adverse event
Study Start Date
March 2008 (undefined)
Primary Completion Date
April 2009 (Actual)
Study Completion Date
April 2011 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Cantonal Hospital of St. Gallen

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The aim of this study is to investigate the effect of the implantation of an Ultrapro® Mesh as prevention of incisional hernia after elective open abdominal aortic aneurysm repair. According to the literature these patients have an increased risk for an incisional hernia. By the implantation of an artificial mesh into the abdominal wall during the first abdominal aortic aneurysm repair, the risk can be reduced dramatically. In small feasibility studies incisional hernia rates as low as 0% have been achieved. Patients scheduled for elective open abdominal aortic aneurysm repair will be randomized into two groups, one receiving an onlay mesh, the other conventional wound closure with sutures.
Detailed Description
Prospective randomized controlled study with two study arms. Arm 1: Abdominal wall will be closed with a prophylactic mesh implantation in onlay technique after elective open abdominal aortic aneurysm repair. Arm 2: Abdominal wall will be closed with standard sutures (without mesh implantation) After the patients gave their informed consent to participate in the study, they will be randomized to one of the two treatment arms. Allocation is carried out based on a prepared randomization list. Primary endpoint is the rate of incisional hernias within the follow-up period of 2 years. Secondary endpoints are postoperative complications and adverse events during the follow-up period. Study enrollment was prematurely terminated on 30. Apr 2009. Already enrolled patients will be followed for 24 months according to protocol.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Abdominal Aortic Aneurysm
Keywords
Abdominal aortic aneurysm, Abdominal hernia

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
9 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Mesh implantation
Arm Type
Experimental
Arm Description
Ultrapro® Mesh implantation
Arm Title
Standard wound closure without a mesh
Arm Type
Active Comparator
Arm Description
Standard wound closure
Intervention Type
Device
Intervention Name(s)
Ultrapro® Mesh implantation
Intervention Description
After the aortic procedure (aortic aneurysm repair) an Ultrapro absorbable mesh will be used for the wound closure of the abdominal wall using an onlay technique.
Intervention Type
Other
Intervention Name(s)
Standard wound closure
Intervention Description
Abdominal closure will be performed with standard sutures without a mesh.
Primary Outcome Measure Information:
Title
Incidence of incisional hernia
Time Frame
24 months
Secondary Outcome Measure Information:
Title
Rate of postoperative complications
Time Frame
7 days
Title
operation time
Time Frame
4 hours
Title
Rate of adverse events
Description
Adverse events related to mesh implantation
Time Frame
24 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patient scheduled for elective or early elective open repair of aortic aneurysm Exclusion Criteria: Emergency surgery EVAR (endovascular procedure) Patients with previous midline laparotomy Patients with in situ abdominal mesh after previous hernia repair Patients with large diastasis of abdominal wall Allergy to penicillin Women before menopause (mesh can interfere with potential future pregnancies)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Wolfgang Nagel, MD
Organizational Affiliation
KSSG
Official's Role
Principal Investigator
Facility Information:
Facility Name
Kantonsspital St. Gallen, Department of Surgery
City
St. Gallen
State/Province
Saint Gallen
ZIP/Postal Code
9007
Country
Switzerland

12. IPD Sharing Statement

Links:
URL
http://www.surgery.ch
Description
Homepage of the Department of Surgery, Cantonal Hospital St. Gallen (KSSG)

Learn more about this trial

Prevention of Incisional Hernia After Elective Open Abdominal Aortic Aneurysm (AAA) Repair

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