Breast Cancer Clinical Trial

Comparison of Pre-op and Post-op Pectoralis Nerve Block

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.

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Full 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.

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Eligibility Criteria

Inclusion Criteria:

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

Exclusion Criteria:

More than 80 years of age
Male
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

Study is for people with:

Breast Cancer

Estimated Enrollment:

35

Study ID:

NCT03653988

Recruitment Status:

Completed

Sponsor:

Melinda Seering

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There is 1 Location for this study

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University of Iowa Hospitals and Clinics
Iowa City Iowa, 52245, United States

How clear is this clinincal trial information?

Study is for people with:

Breast Cancer

Estimated Enrollment:

35

Study ID:

NCT03653988

Recruitment Status:

Completed

Sponsor:


Melinda Seering

How clear is this clinincal trial information?

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