Breast Pain Clinical Trial
Official title:
Analgesic Effects of Local Anesthetic Serratus Plane Infiltration for Total Mastectomy Surgery: A Pilot Study
Pain following mastectomy surgery for breast cancer can be significant. Poorly managed pain in the immediate time-period following surgery can potentially lead to long-term (chronic) pain conditions. There is still a need to find the safest, least invasive, and most effective method to manage this pain. The investigators believe that a new technique of injecting local anesthesia (freezing) in to specific areas at the end of mastectomy surgery may be a very important step to managing pain after breast surgery. The investigators would like to begin by performing a pilot study, meaning the investigators will perform the technique in patients and compare what their pain outcomes are to patients who have not had the technique.
Status | Not yet recruiting |
Enrollment | 40 |
Est. completion date | December 2016 |
Est. primary completion date | December 2016 |
Accepts healthy volunteers | No |
Gender | Female |
Age group | 18 Years to 85 Years |
Eligibility |
Inclusion Criteria: - Undergoing elective or urgent, primary, unilateral mastectomy with or without axillary lymph node dissection - ASA-PS I-III - 18-85 years of age, inclusive - 50-100 kg, inclusive - BMI 18 - 40 Exclusion Criteria: - Bilateral mastectomy surgery - Revision mastectomy surgery - Inability or refusal to provide informed consent - Chronic pain state - Neuropathic pain - Opioid dependence - Allergy to local anesthesia - Allergy to opioids |
Allocation: Non-Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
University Health Network, Toronto |
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change in subjective Visual Analogue Scale (VAS) | The visual analogue scale is administered at different time points | 7 days after surgery | No |
Secondary | Patient Adverse Event Outcomes | The visual analogue scale is administered at different time points | 72 hours post operatively | No |
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