Clinical Trials Logo

Clinical Trial Summary

This multicenter randomized controlled non-inferiority trial of only mesh fixation with a glue applicator is a trial to evaluate the outcomes between atraumatic laparoscopic mesh fixation with GLUTACK-Glubran2® and conventional traumatic fixation, so the primary endpoint of the study is to analyze the recurrence on ventral or incisional hernia repair 2 years postoperatively assessed by a clinical and/or imaging technique.


Clinical Trial Description

Patients older than 18 years undergoing an elective ventral/incisional hernia laparoscopic repair with a hernia defect between 4-10cm of transversal defect The patients included are adults with a BMI lesser than 35 Kg/m2 undergoing an elective laparoscopic primary ventral or incisional hernia repair with a fascial transverse defect between 4-8 cm (W2 EHS) on anterior or lateral location (M1-M5 up to 10 cm of length or L1-3) For the interventional procedure, three ports are used (1x11 mm and 2x5 mm) and after adhesiolysis and the field prepared, the defect is measured with a local standard in a craneo-caudal and transversal directions. Then, the defect is closed with a 2-0 caliber barbed suture following its biggest axis. A Dynamesh IPOM previously hydrated (2-3 min) is introduced throughout the 11mm trocar and extended. After this maneuver, mesh fixation is performed depending on the randomized arm (125 per arm): either traumatic fixation with the conventional procedure and device or with Glutack-Glubran®2. After two years of follow-up, the recurrence will be analyzed. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06183840
Study type Interventional
Source Institut Catala de Salut
Contact
Status Not yet recruiting
Phase N/A
Start date March 10, 2024
Completion date December 31, 2026

See also
  Status Clinical Trial Phase
Terminated NCT03034213 - Gentrix™ Versus Biological or Prosthetic Mesh N/A
Enrolling by invitation NCT06306976 - Shear-Wave Elastography N/A
Completed NCT02206828 - The SymCHro - Observational Registry Study for Symbotex™ Composite Mesh in Ventral Hernia Repair
Not yet recruiting NCT04624100 - Quality Control of Ventral Hernia Surgery by Prospective Registration
Active, not recruiting NCT03324854 - Use of Mosquito Net Mesh for Ventral Hernia Repair N/A
Not yet recruiting NCT05575141 - Robotic Versus Open Comparison in the Surgical Treatment of Wide Abdominal Wall Hernias N/A
Completed NCT01325792 - Open Complex Ventral Incisional Hernia Repair Using Biosynthetic Material for Midline Fascial Closure Reinforcement N/A
Terminated NCT03317665 - Observational Biologic or Prosthetic Mesh
Recruiting NCT05576753 - Preperitoneal Umbilical Mesh Area N/A
Completed NCT05142761 - Tension in Posterior Component Separation for Abdominal Wall Reconstruction
Recruiting NCT03255239 - Open Preperitoneal Mesh Versus Retromuscular Mesh Versus Suture Repair for Abdominal Wall Hernias N/A
Completed NCT03043079 - Ultrasound Assessment of Ventral Hernia Defects N/A
Completed NCT02129140 - Observational Study to Evaluate Ventral Incisional Hernia Repair Using a Biologic Mesh (Cook Biodesign)