Multimodal Narcotic Limited Perioperative Pain Control With Colorectal Surgery

Status unconfirmed · Phase 4

Conditions studied: Colon Cancer, Colon Diverticulosis, Colonic Neoplasms, Colonic Diverticulitis, Pain, Postoperative, Ileus, Ileus Paralytic, Ileus; Mechanical, Constipation Drug Induced, Constipation, Rectum Cancer, Rectum Neoplasm

In brief

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.

Key facts

Study ID

NCT02958566

Run by

University of Illinois College of Medicine at Peoria

People needed

80

Starts

2017-01-01

Expected to finish

2018-12-01

Last updated by the study team

2017-03-20

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Males or females above the age of 18
• Patients undergoing laparoscopic or robotic colorectal resections

You may not qualify if…

• 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.

Where it is running

• Uicomp — Peoria, Illinois, United States (enrolling)

Full record on ClinicalTrials.gov

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