UnknownPhase 4ketamine
Multimodal Narcotic Limited Perioperative Pain Control With Colorectal Surgery
Sponsored by University of Illinois College of Medicine at Peoria
NCT ID
NCT02958566
Target Enrollment
80 participants
Start Date
2017-01
Est. Completion
2018-12
About This Study
The General Objective of this study is to investigate the cost and efficacy of treating patients undergoing colorectal surgical resections with an opioid limited pain control regimen as part of an Enhanced Recovery After Surgery (ERAS) Protocol. This group will be compared to a traditional opioid based pain control regimen.
Conditions Studied
Interventions
- •Acetaminophen
- •Gabapentin
- •Orphenadrine
- •Lidocaine
- •Marcaine
- •Ketamine
- •Methadone
- •Tramadol
- •Ketorolac
- •Morphine Sulfate
- •Fentanyl
- •Dilaudid
- •Hydrocodone-Acetaminophen Tab 5-325 MG
- •Morphine Sulfate
- •Fentanyl
- •Dilaudid
- •HYDROCODONE/ACETAMINOPHEN 5 Mg-325 Mg ORAL TABLET
Eligibility
Age:18 Years - N/A
Healthy Volunteers:No
View full eligibility criteria
Inclusion Criteria: * Males or females above the age of 18 * Patients undergoing laparoscopic or robotic colorectal resections Exclusion Criteria: * History of constipation * Pre-existing use of narcotics or opioids * Pre-existing renal or hepatic failure * Mental illness, mental retardation, or inability to participate in informed consent due to mental status * Pre-existing dementia * Allergy to any protocol medication * Emergency operation * Subjects who are incarcerated or wards of the state * Minors * Subjects with inflammatory bowel disease, active colitis, or pre-existing intra-abdominal inflammation. Diverticulitis without active infection/inflammation will not be excluded.
Study Locations (1)
Uicomp
Peoria, Illinois, United States