Pain Clinical Trial - Use of On-Q Pump for Pain Post C-Section

Status Completed

Clinical Trial Summary

Clinical Trial Description

The main purpose of this study is to examine if pain levels treated with intrathecal (IT) preservative-free morphine (PFM) after a cesarean section improve with the additional use of continuous subfascial wound infiltration with ropivacaine using the OnQ® elastomeric pump system. As a double-blinded, randomized, placebo controlled study, women undergoing first, second or third cesarean section will be randomly assigned to one of 3 different groups. Group 1 will receive saline, group 2 will be given ropivacaine 0.1%, group 3 will be given ropivacaine 0.2%, all at a rate of 8ml/hr via the OnQ® pump system. Each group will also receive an 8mL bolus of the previously assigned infusate. The investigator will assess pain at rest and with movement at different time periods during the recovery process through 3 months post operatively. The investigator will also assess if the use of this system decreases the need for other pain medications and reduces the potential side-effects of pain treatment. ;

Study Design

Related Conditions & MeSH terms

Pain

Clinical Trial Details

NCT number	NCT02579629
Study type	Interventional
Source	Emory University
Contact
Status	Completed
Phase	Phase 4
Start date	July 2015
Completion date	July 25, 2019

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