Clinical Trials Logo

Clinical Trial Summary

Ventral hernias in the midline of the abdominal wall are one of the most frequent diseases in general and visceral surgery worldwide. The optimal operative technique is still in discussion. The traditional techniques are open sublay or transabdominal intraperitoneal onlay mesh (IPOM) repair. In order to avoid the risks -large trauma to the abdominal wall with pain and infection, lesion of intraabdominal organs - a new hybrid technique - small skin incision, wide endoscopic dissection of the retrorectus space with implantation of a large mesh - was developed (EMILOS -Endoscopic Mini/Less Open Sublay).


Clinical Trial Description

Long-term results in 174 patients with a ventral hernia of the abdominal wall after EMILOS (Endoscopic Mini/Less Open Sublay) repair. The worldwide most frequently used surgical techniques to repair ventral abdominal wall hernias are the open sublay operation and the transabdominal IPOM (Intra-Peritoneal Onlay Mesh) technique. Therefore a special questionnaire was developed to send to the patients to evaluate long-term outcome. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05912868
Study type Observational
Source Diakonie-Klinikum Stuttgart
Contact
Status Completed
Phase
Start date June 25, 2015
Completion date December 31, 2022

See also
  Status Clinical Trial Phase
Recruiting NCT06051578 - Abdominal Wall Tension in Patients Undergoing Ventral Hernia Repair Without Component Separation
Recruiting NCT04098380 - Small Versus Large Bite Closure of Emergency Midline Laparotomy N/A
Completed NCT02616718 - Incisional Hernia Progression Over Time N/A
Completed NCT06034652 - T-GENVIH-003 LTFU (Long Term Follow Up) Study
Completed NCT04222517 - The Use of Local Hemostatic in Patients With Large Incisional Hernias N/A
Completed NCT00749268 - AbsorbaTack Evaluation of Postoperative Pain Following Laparoscopic Hernia Repair Phase 4
Not yet recruiting NCT05467124 - Enhanced Recovery After Abdominal Wall Reconstruction
Completed NCT00472537 - ProLOVE - Prospective Randomized Study of Midline Incisional Hernia Treatment N/A
Active, not recruiting NCT02365194 - Modifying Risk in Ventral Hernia Patients N/A
Recruiting NCT04718168 - GORE® ENFORM Biomaterial Product Study N/A
Completed NCT02594241 - PreOperative Steroid in Abdominal Wall Reconstruction: A Double-blinded Randomized Clinical Trial N/A
Active, not recruiting NCT02363790 - Primary Fascial Closure With Laparoscopic Ventral Hernia Repair: A Randomized Controlled Trial N/A
Completed NCT02398565 - Pregnancy Subsequent to Ventral Hernia Repair N/A
Terminated NCT02041494 - Complex Ventral Hernia Repair Using Biologic or Synthetic Mesh N/A
Completed NCT00532870 - Laparoscopic Intraperitoneal Mesh Repair of Ventral Hernia: Comparison to Conventional Mesh Repair N/A
Completed NCT05320055 - Pain and Readmission After Lap IPOM vs. Robotic Ventral Hernia Repair
Completed NCT04229940 - Peritoneal in Laparoscopic Ventral Hernia Repair 2 Phase 2
Completed NCT05446675 - Endoscopic eTEP Versus Open Rives-Stoppa
Withdrawn NCT04143776 - Renal- and Pulmonary Function in Relation to Abdominal Hypertension After Abdominal Reconstruction
Active, not recruiting NCT02457364 - Non-Op Management of Ventral Hernia Patients