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The Mesh-RTL Project, for Prevention of Incisional Hernia (RTL)

Primary Purpose

Hernia Incisional

Status
Completed
Phase
Not Applicable
Locations
Mexico
Study Type
Interventional
Intervention
Mesh reinforcement
RTL reinforcement
Sponsored by
Hospital Regional de Alta Especialidad del Bajio
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Hernia Incisional focused on measuring Mesh, RTL(reinforced tension line), Prevention, Prophylactic Mesh

Eligibility Criteria

18 Years - 70 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Patients older than 18 years undergoing midline laparotomy, independently of diagnostic or condition, elective or emergency surgery
  • Patients with a score equal or greater than 7 of the hernia score
  • Patients who accept to participate and sign the informed consent

Exclusion Criteria:

  • Patients managed with open abdomen or with the impossibility of close the wall
  • Patients who had a previous incisional hernia or patients who are participing in anohter trial
  • Patients with a life expectative less than 12 months
  • Pregnant patients Patients with the antecedent of rejection of prosthesic material

Sites / Locations

  • Hospital regional de Alta Especialidad del bajio

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

Onlay Mesh Reinforcement group

RTL reinforcement group

Arm Description

The midline fascia was closed with running, slowly absorbable sutures (PDS 1-0) with a recommended suture length to wound length ratio of 4:1. An anterior plane with a width of about 8 cm was created between the anterior fascia and the subcutis. A Lightweight polypropylene mesh was used and placed on the anterior rectus fascia with an overlap of 3 cm. The mesh was fitted in the dissected space and it was fixed with PDS 2-0 suture. Fixing points are placed taking the mesh and the anterior fascia of the rectus muscle, at a distance of 3 cm between each point until completing its circunference.

The RTL suture is placed parallel at a distance of 0.5 cm from the fascial margin. Ideally the thread should lie between the anterior and the posterior rectus muscle sheath; there should be no contact with the rectus muscle. A nonabsorbable monofilamental polypropylene thread and a 65-mm ½ needle are used. Around this longitudinal thread, the continuous suture for fascial closure is introduced immediately lateral to the thread; with running, slowly absorbable sutures (PDS 1-0) with a recommended suture length to wound length ratio of 4:1. An anterior plane with a width of about 8 cm was created between the anterior fascia and the subcutis

Outcomes

Primary Outcome Measures

Number of participants with acute incisional hernia
An abdominal wall gap with or without bulge in the area of the postoperative scar palpable bi clinical examination (yes or not)
Number of participants with Incisional hernia
An abdominal wall gap with or without bulge in the area of the postoperative scar palpable bi clinical examination (yes or not)
Number of participants with Incisional hernia
An abdominal wall gap with or without bulge in the area of the postoperative scar palpable bi clinical examination (yes or not)

Secondary Outcome Measures

Number of participants with surgical site infection
Includes at least one of the following: (a) purulent drainage is present (culture documentation not required); (b) organisms are isolated from fluid/tissue of the superficial incision; (c) at least one sign of inflammation (eg, pain or tenderness, induration, erythema, local warmth of the wound) is present; (d) the wound is deliberately opened by the surgeon; (e) the surgeon or clinician declares the wound infected
abdominal pain postoperative
It will be measured according to the visual analogue scale. Scale whose score goes from 0-10 being ten the maximum level expressed by the patient.
Number of participants with seroma
presence of accumulation of clear body fluids in a place where the tissue has been removed by surgery, not associated with infection

Full Information

First Posted
October 8, 2019
Last Updated
February 9, 2022
Sponsor
Hospital Regional de Alta Especialidad del Bajio
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1. Study Identification

Unique Protocol Identification Number
NCT04134455
Brief Title
The Mesh-RTL Project, for Prevention of Incisional Hernia
Acronym
RTL
Official Title
The Mesh-RTL Project for Prevention of Incisional Hernia: Clinical Trial of Non-inferiority to Compare Two Aponeurotic Closure Techniques in Midline Laparotomy in Patients With Elevated Risk for Hernia
Study Type
Interventional

2. Study Status

Record Verification Date
February 2022
Overall Recruitment Status
Completed
Study Start Date
January 20, 2022 (Actual)
Primary Completion Date
January 30, 2022 (Actual)
Study Completion Date
February 4, 2022 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Hospital Regional de Alta Especialidad del Bajio

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Introduction: By definition, the laparotomy is a surgical incision into the abdomen cavity performed to examine the abdominal and retroperitoneal organs. The evisceration/eventration and the hernia are considered the most frequent complication of the midline laparotomy with a high morbidity and mortality related. Conditions that will require a second intervention, in Mexico represent the seventh cause of elective surgery and fourth cause of emergency procedures. The objective of this study is to determine if the incidence of post-incisional hernia in patients with high risk after a midline laparotomy are similar between the closure of the abdominal wall with the RTL technique and the supraaponeurotic mesh closure reinforcement. Material and Methods: Clinical trial comparing the use of mesh against the RTL technique for post-incisional hernia prophylaxis. Two groups, triple blind Analysis will be carried out with intent to treat and not inferiority with 95% confidence intervals
Detailed Description
Introduction: By definition, the laparotomy is a surgical incision into the abdomen cavity performed to examine the abdominal and retroperitoneal organs. It is classified according to the medical indication: exploratory, therapeutic, stagemaker, and recently added "damage-control" laparotomy. There exists so many ways to access the abdominal cavity, usually in relation with the organ or structure to treat; being classified in midline laparotomy, paramedian, transversal, oblique, abdominal-thoracic, etc. Either an emergency or scheduled procedure, the more usual and functional continues being the midline laparotomy, since it allows a broader and faster approach, with less bleeding and easily to extend if it becomes necessary. Both the evisceration/eventration and the hernia are considered the most frequent complication of the midline laparotomy with a high morbidity and mortality related. Conditions that will require a second intervention, in Mexico represent the seventh cause of elective surgery and fourth cause of emergency procedures. So far only the use of the mesh has proven useful in reducing this complication. The authors published in 2016 a clinical trial where it showed that the technique is safe and effective to reduce the presence of incisional hernia, however the use of the mesh brings with it problems such as cost, possibility and use in contaminated cavities and postoperative pain. Therefore, the use of the RTL technique as an alternative means to this will help to have one more option for the management of patients with a high risk of incisional hernia. Problem Statement: Does the RTL closing technique in the midline laparotomy has the same incident of herniation than the close with supraaponeurotic mesh in patient with elevated risk? Justification The presence of postincisional hernia need to be considerate as a serious disease, insomuch as it carry on highs rates of morbimortality. The presence of this eventuality is among 0.4-1.2% in elective surgery and up to 30% in emergency procedures. It is calculated in de U.S.A. an approximate of 1 million of reinterventions a year to correct this condition, with the respective monetary, time and suffering cost to the patient and the health system. Given the seriousness, the ultimate global consensus has determinate three main axes to the surgical community to board: Identify the relevance of the problem Improve the theoretical knowledge and technical capacity in the closing of the abdominal wall Implement prophylactic measures in the patients, especially in those with elevated risk. With the present study the authors aim to contribute to this global recommendations, comparing two closing techniques of the abdominal wall after a midline laparotomy in patients with elevated risk of herniation. Both techniques are proved safe and useful in other studies, with no comparison to date. Demonstrate that the use of RTL technique has a similar incidence of herniation than the mesh, in an attempt to prevent postincisional hernias after a midline laparotomy, will bring to the surgical community a cheaper and practical alternative to the mesh. Objectives: General: To determinate if the incidence of post-incisional hernia in patients with high risk after a midline laparotomy are similar between the closure of the abdominal wall with the RTL technique and the supraaponeurotic mesh closure reinforcement. Specifics: To identify the patients with high risk using de validated HERNIA-Project Score. To determinate the incidence of post-incisional hernia after one year of the initial midline laparotomy. To compare the incidence of post-incisional hernia between the two groups. To describe the complications related to each closure technique. Hypothesis: Ho Hypothesis: There is no difference in the incidence of post-incisional hernia between the RTL technique and the reinforcement with supraaponeurotic mesh closure wall. H1 Hypothesis: There is difference in the incidence of post-incisional hernia between the RTL technique and the reinforcement with supraaponeurotic mesh closure wall. Sample size: The sample size was calculated according to the formula published by Bouemn et all 2015, and based on the results of Kholer and collaborators 2019, where the authors found in which a percentage of success was estimated with the standard treatment of 7% compared to the experimental management of 11%, with a margin of no less than 5%, with an alpha for a tail of 0.05%, and a beta of 20 %, a total of 125 patients per group was obtained. Statistical analysis: Categorical values will be present as frequency and percentage, comparisons between groups will be done using the χ2 test for binary data or Fisher´s exact test. Continuous variables will be presented as means (SDs) or median and range interquartile range, if they meet normal criteria and will be compared using the Mann-Whitney U-test or t student test. p-Values of less than 0.05 will be considered significant. Statistical analyses will be performed using SPSS statistical software, version 25.0.0 (IBM corp). Analysis by intention to treat will be used. A Kaplan-Meier curve of the occurrence of incisional hernias stratified by treatment group will be plotted, and a long-rank test will be used to compare the hernia incidence between the groups

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hernia Incisional
Keywords
Mesh, RTL(reinforced tension line), Prevention, Prophylactic Mesh

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Clinical trial of non-inferiority
Masking
ParticipantInvestigator
Masking Description
The participant and investigator are masked
Allocation
Randomized
Enrollment
250 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Onlay Mesh Reinforcement group
Arm Type
Active Comparator
Arm Description
The midline fascia was closed with running, slowly absorbable sutures (PDS 1-0) with a recommended suture length to wound length ratio of 4:1. An anterior plane with a width of about 8 cm was created between the anterior fascia and the subcutis. A Lightweight polypropylene mesh was used and placed on the anterior rectus fascia with an overlap of 3 cm. The mesh was fitted in the dissected space and it was fixed with PDS 2-0 suture. Fixing points are placed taking the mesh and the anterior fascia of the rectus muscle, at a distance of 3 cm between each point until completing its circunference.
Arm Title
RTL reinforcement group
Arm Type
Experimental
Arm Description
The RTL suture is placed parallel at a distance of 0.5 cm from the fascial margin. Ideally the thread should lie between the anterior and the posterior rectus muscle sheath; there should be no contact with the rectus muscle. A nonabsorbable monofilamental polypropylene thread and a 65-mm ½ needle are used. Around this longitudinal thread, the continuous suture for fascial closure is introduced immediately lateral to the thread; with running, slowly absorbable sutures (PDS 1-0) with a recommended suture length to wound length ratio of 4:1. An anterior plane with a width of about 8 cm was created between the anterior fascia and the subcutis
Intervention Type
Procedure
Intervention Name(s)
Mesh reinforcement
Other Intervention Name(s)
Prophylactic Mesh reinforcement
Intervention Description
Once the surgery is over. The closure is made with the 4: 1 rule, then an onlay mesh is placed that exceeds 3 cm on each side the wound is fixed with suture.
Intervention Type
Procedure
Intervention Name(s)
RTL reinforcement
Other Intervention Name(s)
Technique RTL
Intervention Description
Once the surgery is finished, the ared is reinforced by placing a longitudinal suture parallel to the edge of the wound 0.5 cm, then the wound is closed with a 4: 1 rule but the suture enters lateral to the reinforcement suture
Primary Outcome Measure Information:
Title
Number of participants with acute incisional hernia
Description
An abdominal wall gap with or without bulge in the area of the postoperative scar palpable bi clinical examination (yes or not)
Time Frame
30 days
Title
Number of participants with Incisional hernia
Description
An abdominal wall gap with or without bulge in the area of the postoperative scar palpable bi clinical examination (yes or not)
Time Frame
1 year
Title
Number of participants with Incisional hernia
Description
An abdominal wall gap with or without bulge in the area of the postoperative scar palpable bi clinical examination (yes or not)
Time Frame
3 years
Secondary Outcome Measure Information:
Title
Number of participants with surgical site infection
Description
Includes at least one of the following: (a) purulent drainage is present (culture documentation not required); (b) organisms are isolated from fluid/tissue of the superficial incision; (c) at least one sign of inflammation (eg, pain or tenderness, induration, erythema, local warmth of the wound) is present; (d) the wound is deliberately opened by the surgeon; (e) the surgeon or clinician declares the wound infected
Time Frame
30 days
Title
abdominal pain postoperative
Description
It will be measured according to the visual analogue scale. Scale whose score goes from 0-10 being ten the maximum level expressed by the patient.
Time Frame
5 days postoperative
Title
Number of participants with seroma
Description
presence of accumulation of clear body fluids in a place where the tissue has been removed by surgery, not associated with infection
Time Frame
10 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Patients older than 18 years undergoing midline laparotomy, independently of diagnostic or condition, elective or emergency surgery Patients with a score equal or greater than 7 of the hernia score Patients who accept to participate and sign the informed consent Exclusion Criteria: Patients managed with open abdomen or with the impossibility of close the wall Patients who had a previous incisional hernia or patients who are participing in anohter trial Patients with a life expectative less than 12 months Pregnant patients Patients with the antecedent of rejection of prosthesic material
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jose de Jesus Alvarez Canales, Dr
Organizational Affiliation
Hospital Regional de Alta Especialidad del Bajio
Official's Role
Study Director
Facility Information:
Facility Name
Hospital regional de Alta Especialidad del bajio
City
Leon
State/Province
Guanajuato
ZIP/Postal Code
37660
Country
Mexico

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
Database available for analysis
IPD Sharing Time Frame
2 years
IPD Sharing Access Criteria
previous sending of email requesting it
Citations:
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The Mesh-RTL Project, for Prevention of Incisional Hernia

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