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Clinical Trials/NCT03653988
NCT03653988
Completed
Not Applicable

Analgesia Efficacy of Pre-operative and Post-operative PEC I/II Block for Bilateral Mastectomy With Reconstruction

Melinda Seering1 site in 1 country34 target enrollmentMarch 12, 2019

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Breast Cancer
Sponsor
Melinda Seering
Enrollment
34
Locations
1
Primary Endpoint
Pain Score Assessment Using a Visual Analog Scale-Immediately Post-surgery
Status
Completed
Last Updated
last year

Overview

Brief Summary

The investigators will compare whether patients will have better pain control if they were to receive (PEC I/II block) before surgery or after mastectomy.

Detailed Description

The current standard of care at the University of Iowa is to receive a pectoralis nerve block (PEC I/II) prior to surgery for mastectomy and reconstruction cases. The investigators will compare whether patients will have better pain control if they were to receive (PEC I/II block) before surgery or after the mastectomy. Patients undergoing mastectomies at the University of Iowa Hospitals clinics receive general anesthesia and a regional block for pain control. The most commonly employed regional anesthetic technique is a PECS I/II block to anesthetize the pectoral, intercostobrachial, third to sixth intercostal and long thoracic nerves. The PECS I/II blocks are pectoralis field blocks where local anesthetic medication is injected under ultrasound guidance between the tissue planes of pectoralis major and minor muscles (PECS I) and in the plane of the serratus anterior muscle at the level of the third rib (PECS II). The investigators will randomize patients into two groups and blind the patient and the research assistant collecting the data. Group I will have the block performed after induction of general anesthesia and prior to surgical incision by the anesthesiologist. Group II will have the block administered by the surgeon after mastectomy is performed and before reconstruction. On the day of surgery, the investigators will have patients fill out forms to measure pain catastrophizing and depression and anxiety. The investigators would like to measure if there is any difference in postoperative pain scores (visual analogue scale)-immediately post surgery in post-anesthesia care unit (PACU), and then on the admission unit every 4 hours for the first twenty four hours or on discharge (whichever time-point occurs sooner) and will collect the average pain scale of the day on post-op day (POD) 2,3,5 and 7 via patient communication electronic message in RedCap. The investigators will also measure intraoperative and post-operative narcotic use (converted to morphine equivalents), post-operative nausea and vomiting, length of (PACU) stay. In addition the investigators will also collect pain scores and pain catastrophic scale on POD 14 after surgery at their clinic visits to the surgeon. Other data collected will include time taken to perform block, post-operative infection rate and post-operative flap necrosis rate.

Registry
clinicaltrials.gov
Start Date
March 12, 2019
End Date
October 31, 2021
Last Updated
last year
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Sponsor
Melinda Seering
Responsible Party
Sponsor Investigator
Principal Investigator

Melinda Seering

Principle Investigator

University of Iowa

Eligibility Criteria

Inclusion Criteria

  • At least 18 years of age
  • Bilateral mastectomy for breast cancer
  • Undergoing breast reconstruction
  • Must weigh at least 50 kg

Exclusion Criteria

  • More than 80 years of age
  • Prisoners
  • Patients who can't provide their own consent
  • Lumpectomy only patients
  • Patients having prophylactic mastectomies
  • Patient must weigh at least 50 kg
  • Allergies to local anesthetics
  • Patient refusal
  • Patients with a history of bleeding disorders
  • Non-English speaking patients

Outcomes

Primary Outcomes

Pain Score Assessment Using a Visual Analog Scale-Immediately Post-surgery

Time Frame: upon arrival to the recovery room after leaving the operating room

The primary outcome to be assessed is to determine if there is a quantitative difference in post-operative pain scores as a result of the administration of a pre-operative PECS I/II block versus the administration of an intra-operative PECS I/II block (Post mastectomy but prior to breast reconstruction). The visual analog scale is a unidimensional measure of pain used in a diverse adult population. The numeric values are on a continuous scale from 0 to 10 with 0 indicating no pain, 5 being moderate pain and 10 as intense pain.

Secondary Outcomes

  • Measure the Amount of Narcotics Use to Control Pain (Intra-op)(Intra-operative (narcotics given during the operating room time))
  • Pain Score Assessment Using a Visual Analog Scale-Post-operative Surgical Recheck.(Approximately day 14 post surgery)
  • Pain Score Assessment-Post-operative Day 1(Day 1 post surgery)
  • Pain Score Assessment-Post-operative Day 3(Day 3 post surgery)
  • Pain Score Assessment-Post-operative Day 7(Day 7 post surgery)
  • Measure the Amount of Narcotics Use to Control Pain.(PACU (from time patient left operating room until patient is discharged from the recovery area to in-patient unit). The time limit for this is generally 60-90 minutes)
  • Measure the Amount of Narcotics Use to Control Pain (In-patient)(In-patient (from time patient arrives to in-patient unit from the recovery room until discharged home). Generally this was around 24 hours)

Study Sites (1)

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