UnknownPhase 3ketamine

Effect of Multimodal Opioid-free Anesthesia on Return of Bowel Function in Laparoscopic Colorectal Surgery

Sponsored by University of Saskatchewan

NCT ID
NCT04144933
Target Enrollment
60 participants
Start Date
2021-05-15
Est. Completion
2024-08-01

About This Study

The objective of this study is to determine if an opioid-free general anesthetic (OFA) technique utilizing lidocaine, ketamine, dexmedetomidine and magnesium reduce postoperative opioid consumption and speed return of bowel function in patients undergoing elective, laparoscopic, colorectal surgery compared to traditional opioid-containing general anesthetic techniques. It is hypothesized that this intraoperative OFA regimen will reduce postoperative opioid consumption, and expedite return of bowel function in this population.

Conditions Studied

AnesthesiaGeneral AnesthesiaAnalgesics, OpioidOpioid Free AnesthesiaPostoperative IleusColorectal SurgeryLaparoscopic SurgeryAnalgesiaDexmedetomidineLidocaineKetamine

Interventions

  • Acetaminophen, Gabapentin
  • Acetaminophen, Gabapentin
  • Lidocaine 1% Injectable Solution, Dexmedetomidine, Ketamine
  • Dexamethasone, Ondansetron
  • Sevoflurane, Lidocaine 2% Injectable Solution, Ketamine, Dexmedetomidine, Magnesium Sulfate
  • Lidocaine 1% Injectable Solution, Sufentanil
  • Sevoflurane, Sufentanil

Eligibility

Age:18 Years - N/A
Healthy Volunteers:No
View full eligibility criteria
Inclusion Criteria:

* Age \> 18, American Society of Anesthesiology (ASA) class I-III patients scheduled for elective laparoscopic/laparoscopic assisted colorectal surgery

Exclusion Criteria:

* Emergency surgery, open surgery, contraindications to laparoscopic surgery (ie. adhesions, inability to tolerate pneumoperitoneum), American Society of Anesthesiology (ASA) class 4, age \< 18, pregnant or breastfeeding women, significant cardiorespiratory/hepatic/renal disease, allergy to any study drugs, inability to consent, inability to respond to pain assessments, inability to use the patient controlled analgesia device (PCA)

Study Locations (1)

Royal University Hospital
Saskatoon, Saskatchewan, Canada

This trial is not recruiting

This study is currently not accepting new participants.

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Data Source
ClinicalTrials.gov

Last updated from source