Comparison of Whole Mesh and Split Mesh Use in Laparoscopic Inguinal Hernia Repair
Primary Purpose
Hernia, Inguinal
Status
Recruiting
Phase
Not Applicable
Locations
Turkey
Study Type
Interventional
Intervention
Split Mesh
Sponsored by
About this trial
This is an interventional treatment trial for Hernia, Inguinal focused on measuring Laparoscopic Inguinal Hernia, Laparoscopic Hernia, Whole Mesh, Split Mesh, TAP, TEPP, Inguinal hernia
Eligibility Criteria
Inclusion Criteria:
- Clinical or/and radiological diagnosed primary inguinal hernia
- TEP or TAPP surgical methods
Exclusion Criteria:
- Recurrent hernias
- Patients with previous groin operations on same side
- Pregnant women
- Patients who did not accept to participate in the study
- ASA score of 3 or higher,
Sites / Locations
- Istanbul Training and Research HospitalRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Active Comparator
Arm Label
Whole Mesh
Split Mesh
Arm Description
For the patients in the first group, the whole patch will be laid on the area without being fixed.
The patients in the second group will be given a patch of the same size, but partially divided horizontally and wrapped around the spermatic cord.
Outcomes
Primary Outcome Measures
Carolinas Comfort Scale values
Differences in postoperative pain and quality of life(Carolinas Comfort Scale at first month) in patients who use whole meshes and those who use split meshes.
Recurrence rates
Differences in recurrence rates in patients who use whole meshes and those who use split meshes.
Secondary Outcome Measures
Recurrence rates
Difference in recurrence rates at 6 months in patients who use whole meshes and those who use split meshes.
Full Information
NCT ID
NCT05420376
First Posted
May 20, 2022
Last Updated
July 19, 2022
Sponsor
Istanbul Training and Research Hospital
1. Study Identification
Unique Protocol Identification Number
NCT05420376
Brief Title
Comparison of Whole Mesh and Split Mesh Use in Laparoscopic Inguinal Hernia Repair
Official Title
Prospective Comparison of Whole Mesh and Split Mesh Use in Patient Groups Undergoing Laparoscopic Inguinal Hernia Repair
Study Type
Interventional
2. Study Status
Record Verification Date
July 2022
Overall Recruitment Status
Recruiting
Study Start Date
June 16, 2022 (Actual)
Primary Completion Date
May 16, 2023 (Anticipated)
Study Completion Date
June 16, 2023 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Istanbul Training and Research Hospital
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
At least 80 patients who will undergo laparoscopic inguinal hernia repair surgery will be randomized into 2 groups. For the patients in the first group, the whole mesh will be laid on the area without being fixed. The patients in the second group will be given a mesh of the same size, but partially divided horizontally and wrapped around the spermatic cord. Demographic data of patients in both groups, quality of life data(Carolinas Comfort Scale) at postoperative 1st, 7th, 30th, 3rd and 6th months, postoperative pain (VAS values), clinical seroma rate, recurrence and other complications will be monitored. When the desired number of patients and follow-up period are reached, the data in the 2 groups will be compared.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hernia, Inguinal
Keywords
Laparoscopic Inguinal Hernia, Laparoscopic Hernia, Whole Mesh, Split Mesh, TAP, TEPP, Inguinal hernia
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
80 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Whole Mesh
Arm Type
Active Comparator
Arm Description
For the patients in the first group, the whole patch will be laid on the area without being fixed.
Arm Title
Split Mesh
Arm Type
Active Comparator
Arm Description
The patients in the second group will be given a patch of the same size, but partially divided horizontally and wrapped around the spermatic cord.
Intervention Type
Procedure
Intervention Name(s)
Split Mesh
Other Intervention Name(s)
Whole mesh
Intervention Description
TEP repair of inguinal hernias using either split or whole mesh
Primary Outcome Measure Information:
Title
Carolinas Comfort Scale values
Description
Differences in postoperative pain and quality of life(Carolinas Comfort Scale at first month) in patients who use whole meshes and those who use split meshes.
Time Frame
6 month
Title
Recurrence rates
Description
Differences in recurrence rates in patients who use whole meshes and those who use split meshes.
Time Frame
6 month
Secondary Outcome Measure Information:
Title
Recurrence rates
Description
Difference in recurrence rates at 6 months in patients who use whole meshes and those who use split meshes.
Time Frame
6 month
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Clinical or/and radiological diagnosed primary inguinal hernia
TEP or TAPP surgical methods
Exclusion Criteria:
Recurrent hernias
Patients with previous groin operations on same side
Pregnant women
Patients who did not accept to participate in the study
ASA score of 3 or higher,
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Erol Aydın, MD
Phone
+905322546001
Email
erolay@gmail.com
Facility Information:
Facility Name
Istanbul Training and Research Hospital
City
Istanbul
Country
Turkey
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Erol AYDIN, MD
Phone
+90 5322546001
Email
erolay@gmail.com
12. IPD Sharing Statement
Plan to Share IPD
Undecided
Learn more about this trial
Comparison of Whole Mesh and Split Mesh Use in Laparoscopic Inguinal Hernia Repair
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