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Clinical Trials/NCT02741232
NCT02741232
Completed
N/A

Comparison of Perioperative Opioid Consumption Following Pectoral Nerve Block Under General Anesthesia for Breast Cancer Surgery: A Randomized Clinical Trial

Maisonneuve-Rosemont Hospital1 site in 1 country50 target enrollmentMarch 2016

Overview

Phase
N/A
Intervention
Lidocaine 1% with epinephrine 1/400000
Conditions
Nerve Block
Sponsor
Maisonneuve-Rosemont Hospital
Enrollment
50
Locations
1
Primary Endpoint
Intraoperative remifentanil consumption for the first 30 minutes of surgery
Status
Completed
Last Updated
7 years ago

Overview

Brief Summary

In this study, the investigators will compare the intraoperative opioid consumption for patients undergoing breast cancer surgery. The patients will be divided in two groups, the first one will receive a pectoral nerve block right after induction of anesthesia and the second one, the control group, will not receive the pectoral block. Our hypothesis is that the pectoral nerve block reduces the opioid consumption during the surgery.

Detailed Description

After induction of general anesthesia with propofol, remifentanil and succinylcholine, the patients will be divided either in the pectoral block group or the control group (sham block). Both groups will receive the same perioperative and postoperative anesthetic protocol. The investigator in charge of the patient will leave the operative room right before the completion of the pectoral block (or the sham block) to preserve randomisation and the block will be performed by another investigator. The pectoral block is performed under ultrasound guidance with 10 cc of lidocaine 1% with epinephrine 1/400000 between the pectoralis major muscle and the pectoralis minor muscle and 20 cc of the same solution between the pectoralis minor muscle and the serratus anterior muscle at the third rib. Anesthesia will be maintained with sevoflurane for a bispectral (BIS) index between 45 and 60. Analgesia will be provided with a perfusion of remifentanil adjusted to maintain a mean arterial blood pressure (MAP) in the range of ± 10% of the basal MAP (mean of the last three MAPs obtained before surgical incision, under sevoflurane-only anesthesia). The total remifentanil consumption will be assessed and compared between the groups. The investigators believe that the pectoral nerve block will significantly reduce the intraoperative remifentanil consumption.

Registry
clinicaltrials.gov
Start Date
March 2016
End Date
September 15, 2017
Last Updated
7 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Olivier Verdonck

Clinical Assistant Professor

Maisonneuve-Rosemont Hospital

Eligibility Criteria

Inclusion Criteria

  • ASA 1 to 3 inclusively
  • breast cancer surgery with or without axillary dissection

Exclusion Criteria

  • any contraindication to the pectoral nerve block (coagulopathy, infection, pre- existing neuropathy, local anesthetic allergy and refusal of local anesthesia)
  • refusal to participate in the study
  • patient with dementia
  • preoperative breast pain
  • preoperative opioid consumption
  • breast reconstructive surgery
  • bilateral surgery
  • pregnant patient

Arms & Interventions

Pectoral nerve block

After induction of general anesthesia and under ultrasound visual guidance, pectoral block is performed with 30 mL total of local anesthetic (1% lidocaine + 1/400000 epinephrine). 10 mL of local anesthetic between pectoralis major muscle and pectoralis minor muscle and 20 mL between pectoralis minor muscle and serratus anterior muscle at the third rib.

Intervention: Lidocaine 1% with epinephrine 1/400000

Sham block

No needle or injection will be used

Intervention: sham block

Outcomes

Primary Outcomes

Intraoperative remifentanil consumption for the first 30 minutes of surgery

Time Frame: 30 minutes

Secondary Outcomes

  • Postoperative nausea and vomiting evaluation(30 minutes)
  • Postoperative pain evaluation(30 minutes)
  • Total intraoperative remifentanil consumption(2 hours)
  • Total intraoperative sevoflurane consumption(2 hours)
  • Total time in the recovery room(60 minutes)
  • Postoperative opioid consumption(1 hour)

Study Sites (1)

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