Expired Study
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Jacksonville, Florida 32224


Purpose:

This study is prospective, randomized trial in which EXPAREL TAP block is compared to standard IT opioid administration, in relieving postoperative pain, decreasing length of stay, and use of narcotic medication.


Study summary:

Primary Objective To assess efficacy of EXPAREL TAP blocks in improving pain scores for 48 hours postoperatively, and in reducing total oral morphine equivalents (OME) use, compared to standard Intrathecal opioid administration (IT). Secondary Objective Assess the length of stay (LOS), postoperative ileus (POI) incidence, and the use of intravenous patient controlled analgesia (PCA) in patients that had EXPAREL TAP blocs compared to IT.


Criteria:

Inclusion Criteria: - • All patients undergoing elective laparoscopic or open colorectal resections who are eligible for IT, and able to be enrolled in ERP. - Age >18 years - BMI <40 - Ability to understand and read English Exclusion Criteria: - • Not able or unwilling to sign consent. - Currently pregnant or lactating. - Patients with chronic pain, requiring daily opiate use at time of surgery. - Patients intolerant of opiates, NSAIDS, acetaminophen or local anesthetics. - Patients requiring emergent surgery. - Abdominoperineal resections - Any contraindications to neuraxial analgesia (coagulopathy, localized infection at the potential site of injection, pre-existing spinal canal pathology) - Patients with a diagnosis of inflammatory bowel disease


NCT ID:

NCT02356198


Primary Contact:

N/A


Backup Contact:

N/A


Location Contact:

Jacksonville, Florida 32224
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: March 16, 2018

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