Preoperative intravenous meloxicam for moderate-to-severe pain in the immediate post-operative period: a Phase IIIb randomized clinical trial in 55 patients undergoing primary open or laparoscopic colorectal surgery with bowel resection and/or anastomosis.
Jennifer D SilinskyJorge E MarcetVamshi Ruthwik AnupindiSwapna U KarkareDrishti R ShahRandall J MackStewart W McCallumWei DuAlex FreyerLibby K BlackPublished in: Pain management (2020)
Aim: Evaluate safety/efficacy of intravenous meloxicam in a colorectal enhanced recovery after surgery protocol. Methods: Adults undergoing primary open or laparoscopic colorectal surgery with bowel resection and/or anastomosis received meloxicam IV 30 mg (n = 27) or placebo (n = 28) once daily beginning 30 min before surgery. Results: Adverse events: meloxicam IV, 85%; placebo, 93%. Adverse events commonly associated with opioids: 41 versus 61% - including nausea (33 vs 50%), vomiting (19 vs 18%) and ileus (4 vs 18%). Wound healing satisfaction scores (physician-rated), clinical laboratory findings and vital signs were similar in both groups. No anastomotic leaks were reported. Opioid consumption, postoperative pain intensity, length of stay and times to first bowel sound, first flatus and first bowel movement were significantly lower with meloxicam IV versus placebo. Most subjects (>92%) were satisfied with postoperative pain medication. Conclusion: Meloxicam IV was generally well tolerated and associated with decreased opioid consumption, lower resource utilization and functional benefits. Clinical Trial Registration: NCT03323385 (ClinicalTrials.gov).
Keyphrases
- postoperative pain
- chronic pain
- pain management
- minimally invasive
- patients undergoing
- double blind
- clinical trial
- robot assisted
- phase iii
- wound healing
- high dose
- primary care
- high intensity
- randomized controlled trial
- emergency department
- rectal cancer
- placebo controlled
- healthcare
- coronary artery bypass
- neuropathic pain
- early onset
- acute coronary syndrome
- low dose
- drug induced
- percutaneous coronary intervention
- adverse drug