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The Effect of Postoperative Abdominal Binder to Improve Outcomes After Incisional Hernia Repair (INSAB)

Primary Purpose

Incisional Hernia

Status
Withdrawn
Phase
Not Applicable
Locations
Denmark
Study Type
Interventional
Intervention
Abdominal binder
Sponsored by
Hvidovre University Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Incisional Hernia

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • elective, primary and recurrent laparoscopic and open incisional hernia repair hernia with mesh reinforcement
  • fascia defects 6-20 cm measured preoperatively by the surgeon at the out-patient clinic
  • patients between 18-80 years

Exclusion Criteria:

  • expected low compliance (language problems, dementia and abuse etc.)
  • fascia defects >20 cm measured at the preoperative clinical examination.
  • acute operation
  • decompensated liver cirrhosis (Child-Pugh 3-4)
  • patients with a stoma
  • if a secondary operation is performed during the hernia repair procedure.
  • if a patient withdraws his inclusion consent

Sites / Locations

  • Hvidovre University Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

No Intervention

Arm Label

abdominal binder

No abdominal binder

Arm Description

use of postoperative abdominal binder 30 days after the hernia repair

No intervention

Outcomes

Primary Outcome Measures

seroma formation
clinically detectable seroma formation

Secondary Outcome Measures

postoperative pain
Measured with self-registration VAS scales

Full Information

First Posted
January 24, 2013
Last Updated
August 15, 2016
Sponsor
Hvidovre University Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT01776775
Brief Title
The Effect of Postoperative Abdominal Binder to Improve Outcomes After Incisional Hernia Repair
Acronym
INSAB
Official Title
The Effect of Postoperative Abdominal Binder to Reduce Seroma Formation and Improve Early Clinical Outcome After Incisional Hernia Repair.
Study Type
Interventional

2. Study Status

Record Verification Date
August 2016
Overall Recruitment Status
Withdrawn
Why Stopped
due to lack of finace
Study Start Date
January 2016 (undefined)
Primary Completion Date
July 2016 (Actual)
Study Completion Date
August 2016 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Hvidovre University Hospital

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Postoperative seroma formation is one of the most common complications after ventral hernia repair with mesh. Although some seromas may not have clinical impact postoperative seroma formation often causes pain and discomfort and may even compromise wound healing. Abdominal binders (also called trusses, girdle, ostomy belt, longuette or abdominal belt) (AB) are commonly used in abdominal and plastic surgery to prevent seroma formation and diminish pain and discomfort after operation. The primary aim of the present study is to investigate the effect of postoperative abdominal binders after laparoscopic incisional hernia repair on postoperative pain, discomfort and quality of life. Secondary, we register seroma formation. A randomized, controlled, investigator-blinded study supplemented with blinded statistical analysis. We include 60 (2x30) incisional hernia repairs. Patients are randomized either to abdominal binder or no abdominal binder (controls). The abdominal binder is worn from immediately after the operation and continuously for 7 days and nights. All patients have a standardized operation with standardized intra- and postoperative medication regimen. Endpoints measurements are clinically detectable seroma formation scored with seroma classification system buý S. Morales-Conde, pain scored with self-registrations with VAS, and quality of life scored with EQ-5D, recurrence and other complications are also registered. Patients are followed until 90 days after the operation.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Incisional Hernia

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Investigator
Allocation
Randomized
Enrollment
0 (Actual)

8. Arms, Groups, and Interventions

Arm Title
abdominal binder
Arm Type
Active Comparator
Arm Description
use of postoperative abdominal binder 30 days after the hernia repair
Arm Title
No abdominal binder
Arm Type
No Intervention
Arm Description
No intervention
Intervention Type
Device
Intervention Name(s)
Abdominal binder
Other Intervention Name(s)
ETO garments©, ostomy belt, trusses, girdle, longuette, abdominal belt
Intervention Description
The abdominal binder is worn from immediately after the operation and continuously for 7 days and nights. The belts are standard abdominal binders (ostomy belts) from "ETO garments©" with standard height of 22 cm. and five different sizes in width (S, M, L, XL, XXL- depending on waist measure). A fitting will be done for all included patients before the operation by waist measurement according to the recommendation from the company (see below). When applied, the patients are advised to apply the belt in a lying position.
Primary Outcome Measure Information:
Title
seroma formation
Description
clinically detectable seroma formation
Time Frame
30 days postoperatively
Secondary Outcome Measure Information:
Title
postoperative pain
Description
Measured with self-registration VAS scales
Time Frame
pain during the postoperative days 1-3, 7, and 30.
Other Pre-specified Outcome Measures:
Title
Quality of life
Description
measured with EQ-5D
Time Frame
on day 30 and 90 postoperatively
Title
postoperative complications, readmittance, and need for general practitioner visits
Description
30-day complications will be registered by patient interview and by cross-checking patient files and the Danish national patient registry
Time Frame
30 days postoperatively
Title
Cosmetic result
Description
measured with verbal rating scale
Time Frame
3 months postoperatively

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: elective, primary and recurrent laparoscopic and open incisional hernia repair hernia with mesh reinforcement fascia defects 6-20 cm measured preoperatively by the surgeon at the out-patient clinic patients between 18-80 years Exclusion Criteria: expected low compliance (language problems, dementia and abuse etc.) fascia defects >20 cm measured at the preoperative clinical examination. acute operation decompensated liver cirrhosis (Child-Pugh 3-4) patients with a stoma if a secondary operation is performed during the hernia repair procedure. if a patient withdraws his inclusion consent
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Thue Bisgaard, DMSc
Organizational Affiliation
Hvidovre University Hospital
Official's Role
Study Director
Facility Information:
Facility Name
Hvidovre University Hospital
City
Hvidovre
ZIP/Postal Code
2650
Country
Denmark

12. IPD Sharing Statement

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The Effect of Postoperative Abdominal Binder to Improve Outcomes After Incisional Hernia Repair

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