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Comparing Pain After Laparoscopic Hernia Repair Using Two Different Types of Mesh Fixation

Primary Purpose

Inguinal Hernia, Pain

Status
Unknown status
Phase
Not Applicable
Locations
Denmark
Study Type
Interventional
Intervention
Parietex ProGrib self-fixating mesh
Tack fixation
Sponsored by
University of Aarhus
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Inguinal Hernia focused on measuring Inguinal hernia repair, Hernia, ProGrib self-fixating mesh, Biological mesh, Tack fixation

Eligibility Criteria

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

Inclusion Criteria:

  • Patients scheduled for elective, inguinal hernia repair
  • 18 years or older
  • Male gender
  • ASA physical classification system 1-3
  • Informed consent

Exclusion Criteria:

  • Patients with recurrent hernia, except patients operated in childhood without mesh application.
  • Patients with bilateral hernia
  • Patients with chronic pain
  • Patients in anticoagulation therapy
  • Previous major surgery in lower abdomen

Sites / Locations

  • Hospitalsenheden MidtRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

Self-fixating mesh

Tack fixation

Arm Description

During surgery, the Parietex ProGrib mesh will be used.

During surgery, the mesh will be fixated with tacks.

Outcomes

Primary Outcome Measures

Number of patients experiencing acute postoperative pain, using the NRS pain score.
Number of patients with recurrent hernia.

Secondary Outcome Measures

Number of patients experiencing chronic postoperative pain, using the NRS pain score.
Quality of life before and after surgery, using the Carolina Comfort Scale

Full Information

First Posted
June 4, 2015
Last Updated
June 5, 2015
Sponsor
University of Aarhus
Collaborators
Medtronic - MITG
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1. Study Identification

Unique Protocol Identification Number
NCT02467140
Brief Title
Comparing Pain After Laparoscopic Hernia Repair Using Two Different Types of Mesh Fixation
Official Title
A Clinical Study of Postoperative Pain Following Laparoscopic Transabdominal Preperitoneal Inguinal Hernioplasty. Comparing Parietex ProGrib With Tacks for Mesh Fixation
Study Type
Interventional

2. Study Status

Record Verification Date
May 2015
Overall Recruitment Status
Unknown status
Study Start Date
May 2015 (undefined)
Primary Completion Date
May 2016 (Anticipated)
Study Completion Date
May 2017 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Aarhus
Collaborators
Medtronic - MITG

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
A clinical study evaluating acute and chronic pain following laparoscopic inguinal hernia repair comparing the ProGripTM self- fixating mesh with tack fixation.
Detailed Description
The primary aim of this study is to evaluate acute and chronic pain following laparoscopic inguinal hernia repair comparing the ProGripTM self- fixating mesh with tack fixation. The ProGripTM laparoscopic self-fixating mesh has been approved for implantation to reinforce the abdominal wall during laparoscopic inguinal hernia repair (TAPP). The mesh delivers tack free fixation above and below the inguinal ligament potentially eliminating pain associated with traditional tack fixation. The present study is a prospective randomized clinical trial designed to collect information about complications such as acute and chronic pain and hernia recurrence rate from patients referred for laparoscopic inguinal hernia repair. Patients who qualify to take part in the study will be randomized for a procedure using either a self-gripping ProGrip mesh or a conventional polypropylene mesh attached with AbsorbaTackTM. Data will be collected from operations performed at 6 high volume hernia centers in Denmark. Patients eligible for study will be recruited from the referral list for inguinal hernia repair at each participating institution. Prior to scheduled surgery, patients will be consented and will complete a questionnaire on inguinal pain intensity and quality of life . The mesh will be placed intraperitoneally after the component separation is complete. The peritoneal layer will be closed with a V-loc stitch in both groups. After surgery, key clinical data will be recorded, such as type of mesh used, size of the hernia defect, number of tacks used etc. The participating patients will receive postoperative questionnaires following the first year after surgery.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Inguinal Hernia, Pain
Keywords
Inguinal hernia repair, Hernia, ProGrib self-fixating mesh, Biological mesh, Tack fixation

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
500 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Self-fixating mesh
Arm Type
Active Comparator
Arm Description
During surgery, the Parietex ProGrib mesh will be used.
Arm Title
Tack fixation
Arm Type
Active Comparator
Arm Description
During surgery, the mesh will be fixated with tacks.
Intervention Type
Device
Intervention Name(s)
Parietex ProGrib self-fixating mesh
Intervention Description
Laparoscopic transabdominal preperitoneal inguinal hernioplasty using the Parietex ProGrib self-fixating mesh.
Intervention Type
Device
Intervention Name(s)
Tack fixation
Intervention Description
Laparoscopic transabdominal preperitoneal inguinal hernioplasty using the Parietex ProGrib self-fixating mesh using tack fixation.
Primary Outcome Measure Information:
Title
Number of patients experiencing acute postoperative pain, using the NRS pain score.
Time Frame
3 months
Title
Number of patients with recurrent hernia.
Time Frame
1 year
Secondary Outcome Measure Information:
Title
Number of patients experiencing chronic postoperative pain, using the NRS pain score.
Time Frame
1 year
Title
Quality of life before and after surgery, using the Carolina Comfort Scale
Time Frame
6 months

10. Eligibility

Sex
Male
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients scheduled for elective, inguinal hernia repair 18 years or older Male gender ASA physical classification system 1-3 Informed consent Exclusion Criteria: Patients with recurrent hernia, except patients operated in childhood without mesh application. Patients with bilateral hernia Patients with chronic pain Patients in anticoagulation therapy Previous major surgery in lower abdomen
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Malene O Dinesen, MD PhD
Phone
+45 42 29 00 23
Email
maledine@rm.dk
First Name & Middle Initial & Last Name or Official Title & Degree
Marie K Christensen, MD
Phone
+45 40 79 54 59
Email
mariekirk@dadlnet.dk
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Michael F Nielsen, MD PhD
Official's Role
Study Director
Facility Information:
Facility Name
Hospitalsenheden Midt
City
Viborg
State/Province
Region Midt
ZIP/Postal Code
8800
Country
Denmark
Individual Site Status
Recruiting

12. IPD Sharing Statement

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Comparing Pain After Laparoscopic Hernia Repair Using Two Different Types of Mesh Fixation

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