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Use of Human Fibrin Glue Versus Staples for Mesh Fixation in Laparoscopic Transabdominal Preperitoneal Hernioplasty (TISTA)

Primary Purpose

Hernia, Inguinal

Status
Completed
Phase
Not Applicable
Locations
Switzerland
Study Type
Interventional
Intervention
Tissue glue
Staples
Sponsored by
Sascha Müller
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Hernia, Inguinal focused on measuring Hernia, Inguinal

Eligibility Criteria

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

Inclusion Criteria:

  • primary hernia repair (no re-operation for recurrent hernia)
  • good compliance can be expected
  • informed consent

Exclusion Criteria:

  • chronic pain
  • acute pain requiring analgesic others than paracetamol or more than a single dose non-steroidal anti-inflammatory drugs treatment within 48 h before surgery
  • current treatment with psychopharmaceutical drugs
  • mental incapacity
  • known incompatibility (allergies) with the Tisseel compounds

Sites / Locations

  • Cantonal Hospital St.Gallen

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Experimental

Active Comparator

Other

Other

Arm Label

Single sided glue

Single sided stapled

Bilateral glue right

Bilateral glue left

Arm Description

Mesh is fixed with Tisseel for single sided inguinal hernias.

Mesh is fixed with staples for single sided inguinal hernias.

For bilateral inguinal hernias mesh on the right side is fixed with Tisseel, on the left with staples. Experimental treatment and active comparator in the same patient.

For bilateral inguinal hernias mesh on the left side is fixed with Tisseel, on the right with staples. Experimental treatment and active comparator in the same patient.

Outcomes

Primary Outcome Measures

Pain after physical stress
Patient rates his pain on a scale from 0 to 10 (10 equals worst pain imaginable). (NRS numeric rating scale). Patient will be asked to bend the hip joint for 90° on the operated side (both sides for patients with bilateral hernia). Then they are asked for the pain rating (physical stress measurement).

Secondary Outcome Measures

Pain at rest
Patient rates his pain on a scale from 0 to 10 (10 equals worst pain imaginable). (NRS numeric rating scale). Patient is interviewed for pain at rest before pain measurement after physical stress.
Pain after physical stress
Patient rates his pain on a scale from 0 to 10 (10 equals worst pain imaginable). (NRS numeric rating scale). Patient will be asked to bend the hip joint for 90° on the operated side (both sides for patients with bilateral hernia). Then they are asked for the pain rating (physical stress measurement).
Operating time
Time in minutes from the first skin incision to the application of dressing.
Length of hospital stay
Time in days (with one decimal) from start of surgery to hospital release.
Postoperative analgetic requirements
Amount (g/day) and type (paracetamol, metamizol, morphin) of analgesic required after surgery until hospital discharge.
Incidence of persisting pain (neuralgia)
Persisting pain (neuralgia) is defined by the presence of intermittent hyperesthesia, burning sensation or jabbing pain in the ipsilateral inguinal area nerves (genitofemoral nerve, lateral cutaneous femoral nerve, ilioinguinal and iliohypogastric nerve). Evaluation for chronic pain (neuralgia) will be performed during the 1 month follow-up visit. The degree of pain will measured as described above.
Postoperative morbidity
Wound infection (defined as those treated without further surgery and identified by clinical examination without microbiological confirmation) haematoma or seroma formation (identified by clinical examination alone before discharge from hospital, without the requirement for radiological confirmation) Re-operation (Need for re-operation during patients' initial hospital stay) Bleeding Urinary retention, urinary tract infection Pulmonary infection Any serious deviation from the normal postoperative course
Medical leave of absence
Time in days from hospital discharge to first working day. All patients will be encouraged to return to work as soon as possible, irrespective of their profession. Time to return to work will be obtained during 1 month follow-up visit. If still on medical leave of absence at this time, patients will be later contacted by phone to obtain the day of return to work. Depending on the expected course of recovery these calls will be performed in a weekly or biweekly fashion.
Economic impact
Will be calculated using the following factors: Cost for glue, staples and instruments to apply glue or staples If relevant: cost for increased operating time for the "slower" mesh fixation technique length of hospital stay (cost/day) medical leave of absence (converted into a monetary amount using an average salary)

Full Information

First Posted
June 29, 2012
Last Updated
August 7, 2023
Sponsor
Sascha Müller
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1. Study Identification

Unique Protocol Identification Number
NCT01641718
Brief Title
Use of Human Fibrin Glue Versus Staples for Mesh Fixation in Laparoscopic Transabdominal Preperitoneal Hernioplasty
Acronym
TISTA
Official Title
Use of Human Fibrin Glue (Tisseel) Versus Staples for Mesh Fixation in Laparoscopic Transabdominal Preperitoneal Hernioplasty (TISTA)
Study Type
Interventional

2. Study Status

Record Verification Date
August 2023
Overall Recruitment Status
Completed
Study Start Date
January 2013 (undefined)
Primary Completion Date
December 2014 (Actual)
Study Completion Date
December 2015 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Sascha Müller

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Inguinal hernia repairs belong to the most common surgical procedures worldwide. Increasingly they are performed using endoscopical techniques (laparoscopy). Many surgeons prefer to cover the hernia gap with a mesh to prevent recurrence. For it, the mesh must be fixed tightly, but tension free. During laparoscopic surgery the mesh is fixed commonly with staples or tissue glue. However, it is not uncommon that staples cause pain at the staple sites while moving. In addition, staples can cause scarring of the abdominal wall leading to chronic pain. Aim of the study is to provide evidence that mesh fixation with tissue glue causes less postoperative pain compared to fixation with staples. Patients with unilateral inguinal hernia will be randomized to receive either mesh fixation with tissue glue or staples (ratio 1:1). Patients with bilateral inguinal hernia will receive mesh fixation with tissue glue on one side and staple fixation on the other side. The side treated with tissue glue will be randomized (ratio 1:1).
Detailed Description
______________________________________________ The inguinal hernia is the most common hernia, including 90% of all spontaneous hernias, and the inguinal hernia repair is the most frequently performed procedure in general surgery. In the United States more than 700,000 inguinal hernias are repaired annually and in Germany more than 200,000. The standard method for inguinal hernia repair, originally described by Bassini in 1889, is the closure of the inguinal canal using sutures. Due to the high recurrence rate of this technique, methods using the tension-free implantation of synthetic meshes were established. Furthermore, endoscopic/laparoscopy methods were established, in which the hernia canal is usually approached from the posterior side opposite to the anterior site in the open approach. It is still hotly debated which of these approaches and methods is the best. Among the various posterior techniques using preperitoneal mesh implantation, the transabdominal preperitoneal patch plastic repair (TAPP) and the total extraperitoneal (TEP) repair achieved the highest acceptance. There are many indications for the use of both techniques, but the TAPP is recommended especially for recurrent hernias (after open preperitoneal patch plastic) and difficult hernias (sliding or incarcerated hernias). The advantages of the TAPP are that it is easier to perform, has a better possibility of standardization, and offers the option to perform a diagnostic laparoscopy. Thus, the type of hernia can be assessed immediately on both sides and a bilateral repair can be performed without additional incisions. In general, learning TAPP is easier than TEP. Most randomized studies comparing laparoscopic with open repair found the following results for laparoscopy: reduced postoperative pain, earlier return to work, increased costs, increased operating time, longer learning period, and during the early learning phase an increased recurrence and complication rate. In summary open, mesh-based, tension-free repair remains the standard, but laparoscopic herniorrhaphy, in the hands of adequately trained surgeons, produces excellent results comparable to those of open repair. Whether patients suffer from postoperative pain depends on many factors like the type of intervention, complications, age, and individual tolerance. In particular the type of mesh fixation employed during hernioplasty has a strong influence on postoperative pain. In a recent review mesh fixation by glue was compared to mesh fixation with staplers during endoscopic inguinal hernia repair (Surg Laparosc Endosc Percutan Tech (2010) 20:205). For the transabdominal preperitoneal patch plastic repair two randomized controlled trials, one non randomized trial and two case series were identified in this review. Although the authors found reduced postoperative pain and faster recovery after glue fixation without any significant difference in the recurrence rate, the authors still concluded: "As the overall quality of published data remains poor, further well-designed studies are needed until fibrin sealing can replace mechanical stapling as a new standard for mesh fixation." Thus well designed randomized studies comparing glue vs. staples fixation during TAPP are still warranted. Most of the previous studies applied only one mesh fixation method for patients with bilateral hernias. Only one study compared glue and stapler fixation in single patients with bilateral hernias. In this study a 2x2 design will be used, to compare the two fixation methods in patients with unilateral hernia as well as to compare the two methods in the same patient with bilateral hernias, eliminating the interindividual bias of the single hernia group. Furthermore this study focuses on the early postoperative pain, with a rather thorough coverage in the first 2 days. In many other studies the first time pain is measured is one month after surgery, which is the last time point in this study. The main aim of this trial is to investigate the early postoperative pain after laparoscopic hernia repair in TAPP technique using either fibrin glue or staples for mesh fixation.

6. Conditions and Keywords

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

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderOutcomes Assessor
Allocation
Randomized
Enrollment
82 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Single sided glue
Arm Type
Experimental
Arm Description
Mesh is fixed with Tisseel for single sided inguinal hernias.
Arm Title
Single sided stapled
Arm Type
Active Comparator
Arm Description
Mesh is fixed with staples for single sided inguinal hernias.
Arm Title
Bilateral glue right
Arm Type
Other
Arm Description
For bilateral inguinal hernias mesh on the right side is fixed with Tisseel, on the left with staples. Experimental treatment and active comparator in the same patient.
Arm Title
Bilateral glue left
Arm Type
Other
Arm Description
For bilateral inguinal hernias mesh on the left side is fixed with Tisseel, on the right with staples. Experimental treatment and active comparator in the same patient.
Intervention Type
Drug
Intervention Name(s)
Tissue glue
Other Intervention Name(s)
Tisseel (Baxter)
Intervention Description
The mesh fixation for the transabdominal preperitoneal patch plastic repair will be performed with 2 mL of tissue glue.
Intervention Type
Device
Intervention Name(s)
Staples
Other Intervention Name(s)
ProTack (Covidien), Securestrap (Ethicon)
Intervention Description
The mesh fixation for the transabdominal preperitoneal patch plastic repair will be performed with ProTack (Covidien) and Securestrap (Ethicon) staples.
Primary Outcome Measure Information:
Title
Pain after physical stress
Description
Patient rates his pain on a scale from 0 to 10 (10 equals worst pain imaginable). (NRS numeric rating scale). Patient will be asked to bend the hip joint for 90° on the operated side (both sides for patients with bilateral hernia). Then they are asked for the pain rating (physical stress measurement).
Time Frame
24 h after surgery
Secondary Outcome Measure Information:
Title
Pain at rest
Description
Patient rates his pain on a scale from 0 to 10 (10 equals worst pain imaginable). (NRS numeric rating scale). Patient is interviewed for pain at rest before pain measurement after physical stress.
Time Frame
4, 8, 16, 24, 32, 48 h & 1 month after surgery
Title
Pain after physical stress
Description
Patient rates his pain on a scale from 0 to 10 (10 equals worst pain imaginable). (NRS numeric rating scale). Patient will be asked to bend the hip joint for 90° on the operated side (both sides for patients with bilateral hernia). Then they are asked for the pain rating (physical stress measurement).
Time Frame
4, 8, 16, 32, 48 h & 1 month after surgery
Title
Operating time
Description
Time in minutes from the first skin incision to the application of dressing.
Time Frame
4 h
Title
Length of hospital stay
Description
Time in days (with one decimal) from start of surgery to hospital release.
Time Frame
2 weeks
Title
Postoperative analgetic requirements
Description
Amount (g/day) and type (paracetamol, metamizol, morphin) of analgesic required after surgery until hospital discharge.
Time Frame
1 month
Title
Incidence of persisting pain (neuralgia)
Description
Persisting pain (neuralgia) is defined by the presence of intermittent hyperesthesia, burning sensation or jabbing pain in the ipsilateral inguinal area nerves (genitofemoral nerve, lateral cutaneous femoral nerve, ilioinguinal and iliohypogastric nerve). Evaluation for chronic pain (neuralgia) will be performed during the 1 month follow-up visit. The degree of pain will measured as described above.
Time Frame
1 month
Title
Postoperative morbidity
Description
Wound infection (defined as those treated without further surgery and identified by clinical examination without microbiological confirmation) haematoma or seroma formation (identified by clinical examination alone before discharge from hospital, without the requirement for radiological confirmation) Re-operation (Need for re-operation during patients' initial hospital stay) Bleeding Urinary retention, urinary tract infection Pulmonary infection Any serious deviation from the normal postoperative course
Time Frame
1 month
Title
Medical leave of absence
Description
Time in days from hospital discharge to first working day. All patients will be encouraged to return to work as soon as possible, irrespective of their profession. Time to return to work will be obtained during 1 month follow-up visit. If still on medical leave of absence at this time, patients will be later contacted by phone to obtain the day of return to work. Depending on the expected course of recovery these calls will be performed in a weekly or biweekly fashion.
Time Frame
2 months
Title
Economic impact
Description
Will be calculated using the following factors: Cost for glue, staples and instruments to apply glue or staples If relevant: cost for increased operating time for the "slower" mesh fixation technique length of hospital stay (cost/day) medical leave of absence (converted into a monetary amount using an average salary)
Time Frame
2 months

10. Eligibility

Sex
Male
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: primary hernia repair (no re-operation for recurrent hernia) good compliance can be expected informed consent Exclusion Criteria: chronic pain acute pain requiring analgesic others than paracetamol or more than a single dose non-steroidal anti-inflammatory drugs treatment within 48 h before surgery current treatment with psychopharmaceutical drugs mental incapacity known incompatibility (allergies) with the Tisseel compounds
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Sascha A Müller, MD
Organizational Affiliation
Cantonal Hospital St. Gallen
Official's Role
Principal Investigator
Facility Information:
Facility Name
Cantonal Hospital St.Gallen
City
St.Gallen
ZIP/Postal Code
9007
Country
Switzerland

12. IPD Sharing Statement

Citations:
PubMed Identifier
24690207
Citation
Muller SA, Warschkow R, Beutner U, Luthi C, Ukegjini K, Schmied BM, Tarantino I. Use of human fibrin glue (Tisseel) versus staples for mesh fixation in laparoscopic transabdominal preperitoneal hernioplasty (TISTA): a randomized controlled trial (NCT01641718). BMC Surg. 2014 Apr 1;14:18. doi: 10.1186/1471-2482-14-18.
Results Reference
background
Links:
URL
http://www.chirurgie.kssg.ch/home/unsere_klinik.html
Description
Website of the Department of Surgery, Cantonal Hospital St. Gallen (German only)

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Use of Human Fibrin Glue Versus Staples for Mesh Fixation in Laparoscopic Transabdominal Preperitoneal Hernioplasty

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