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
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
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
NCT ID
NCT02467140
First Posted
June 4, 2015
Last Updated
June 5, 2015
Sponsor
University of Aarhus
Collaborators
Medtronic - MITG
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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