Continuous Local Anesthetic Infusion Following Hernia Repair

Status Completed

Clinical Trial Summary

The primary endpoint of this study will determine if subjects receiving a continuous infusion of local anesthetic following laparoscopic ventral hernia repair, with the pain pump installed as described to treat post surgical pain will have a lower incidence of pain than those patients treated with a placebo, saline-filled pain pump.The secondary endpoint of this study will determine if subjects receiving a continuous infusion of local anesthetic following laparoscopic ventral hernia repair, with the pain pump installed as described to treat post surgical pain will have a lower utilization of narcotic analgesic medication than those patients treated with the placebo, saline-filled pain pump.

Clinical Trial Description

Patients will be screened to determine study eligibility using inclusion/exclusion criteria. Following the consent process, subjects will be randomly assigned to a treatment arm (anesthetic or placebo group). Baseline data will be collected prior surgical implantation of the pain pump delivery system. Both study and control groups will be able to receive supplemental medication for breakthrough pain as determined by the surgeon. Post-operative data will be collected up to three weeks following surgery. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT01804114
Study type	Interventional
Source	NorthShore University HealthSystem
Contact
Status	Completed
Phase	N/A
Start date	March 2012
Completion date	October 2015

View Details

See also
Status	Clinical Trial	Phase
Recruiting	`NCT06016426` - Mass Closure vs Layer by Layer Closure	N/A
Recruiting	`NCT05572021` - A Comparison of the Outcomes in Fortiva and Strattice Mesh	N/A
Completed	`NCT02263599` - Conservative Treatment For Ventral Hernia
Completed	`NCT02292264` - Risk Factors and Complications of Ventral Hernia Repair
Completed	`NCT02263625` - Regional Differences In Indication for Ventral Hernia Repair
Completed	`NCT01961687` - A Prospective, Multi-Center Study of Phasix™ Mesh for Ventral or Incisional Hernia Repair.	N/A
Completed	`NCT01325246` - Reoperation Rate Versus Clinical Recurrence After Ventral Hernia Repair	N/A
Completed	`NCT03283982` - Laparoscopic vs. Robotic Ventral Hernia Repair With IPOM	N/A
Not yet recruiting	`NCT05526209` - Longitudinal Relaxing Incision as a Technique for Recurrence Prevention in Ventral Hernia
Completed	`NCT04438369` - Evaluation of Ultrasound-guided Erector Spinae Block for Postoperative Analgesia in Laprascopic Ventral Hernia Repair.	N/A
Recruiting	`NCT04173884` - Video-based Collaborative Learning to Improve Ventral Hernia Repair	N/A
Recruiting	`NCT02703662` - Performance of Biologic Mesh Materials in Abdominal Wall Reconstruction	Phase 2/Phase 3
Completed	`NCT03938688` - Randomized Control Trial Comparing Transfascial Suture for Mesh Fixation to No Mesh Fixation	N/A
Completed	`NCT01719718` - The Influence of Closing the Gap on Postoperative Seroma and Recurrences in Laparoscopic Ventral Hernia Repair	N/A
Completed	`NCT03342040` - Transverse Abdominis Plane Block in Laparoscopic Ventral Hernia Repair	N/A
Completed	`NCT04150796` - Comparing eTEP and Laparoscopic Intraperitoneal Onlay Mesh (IPOM) for Ventral Hernias	N/A
Recruiting	`NCT03222102` - Ventral Hernia Prevention After Liver Transplantation	N/A
Completed	`NCT05610267` - Gentrix® Surgical Matrix for Soft Tissue Reinforcement in Ventral Hernia Repair
Terminated	`NCT01794338` - The Use of Biologic Mesh vs Bioabsorbable Mesh During Ventral Hernia Repair in At-risk Patients	N/A
Completed	`NCT01886963` - A Clinical Trial Using Spy Elite System in Planning Tissue Advancement Flaps After Ventral Hernia Repair	N/A