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

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