Preoperative Regional Nerve Block for Acute and Chronic Post-Operative Pain Following Mastectomy (NCT04019834) | Clinical Trial Compass
CompletedEarly Phase 1
Preoperative Regional Nerve Block for Acute and Chronic Post-Operative Pain Following Mastectomy
United States21 participantsStarted 2020-07-06
Plain-language summary
The purpose of this study is to see if pre-operative regional nerve blocks compared to a placebo nerve block can decrease chronic post mastectomy pain, immediate postoperative pain and postoperative narcotic consumption.
Who can participate
Age range
19 Years
Sex
FEMALE
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion criteria
. Women at least 19 years old who are able to provide written and informed consent
. Women undergoing unilateral or bilateral, simple, skin-sparing, or nipple sparing mastectomy for breast cancer (Stage 0-III) or breast cancer prevention
. Patients with ASA class of I-III will be included
Exclusion criteria
. Stage IV breast cancer, morbid obesity with BMI \>45kg/m2
. Renal insufficiency (Creatinine \>1.5 mg/dL)
. Current chronic analgesic use (daily use for \> or equal to 4 weeks)
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
What they're measuring
1
Postoperative Pain: Brief Pain Inventory- Short Form (BPI-SF)
Timeframe: Baseline (day of surgery) to 8 hours
2
Postoperative Pain
Timeframe: Baseline (day of surgery) to 16 hours (+/- 4 hours)
3
Postoperative Pain: Brief Pain Inventory- Short Form (BPI-SF)
Timeframe: Baseline (day of surgery) to 2 days
4
Postoperative Pain: Brief Pain Inventory- Short Form (BPI-SF)
Timeframe: Baseline (day of surgery) to 14 days (+/- 3 days)
5
Postoperative Pain: Brief Pain Inventory- Short Form (BPI-SF)
Timeframe: Baseline (day of surgery) to 6 months
6
Postoperative Pain: Brief Pain Inventory- Short Form (BPI-SF)