Status:
UNKNOWN
Prospectively Assessing Pain After Breast Surgery
Lead Sponsor:
Cedars-Sinai Medical Center
Conditions:
Pain, Postoperative
Eligibility:
FEMALE
18+ years
Brief Summary
Reducing post-operative pain and reducing the use of opioid narcotics are independently valuable goals. Before studying newer techniques that may help us achieve these goals, we need objective data on...
Detailed Description
Breast surgeons may be able to reduce post-operative pain and the need for opioid narcotics by utilizing regional anesthesia techniques (modified regional blocks) during surgery. To test this hypothes...
Eligibility Criteria
Inclusion
- Provision of signed and dated informed consent form.
- Stated willingness to comply with all study procedures and availability for the duration of the study.
- Female, age 18 or older.
- Scheduled for axillary surgery (sentinel node biopsy or axillary dissection), with or without concurrent lumpectomy.
- Able to take oral narcotics and be willing to adhere to the prescribed regimen.
Exclusion
- A history of chronic pain
- Any previously diagnosed chronic pain syndrome.
- Prior use of narcotics, on more than 5 days in the past 3 months or 10 days in the past year.
Key Trial Info
Start Date :
March 1 2022
Trial Type :
OBSERVATIONAL
Allocation :
ESTIMATED
End Date :
February 28 2025
Estimated Enrollment :
40 Patients enrolled
Trial Details
Trial ID
NCT05210400
Start Date
March 1 2022
End Date
February 28 2025
Last Update
January 27 2022
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