Status:
COMPLETED
Perioperative Systemic Acetaminophen to Improve Postoperative Quality of Recovery After Ambulatory Breast Surgery
Lead Sponsor:
Northwestern University
Conditions:
Pain
Eligibility:
FEMALE
18-70 years
Phase:
NA
Brief Summary
Recent evidence demonstrates that perioperative pain continues to be poorly managed among ambulatory surgical patients. More importantly, few interventions that minimize postoperative pain have also s...
Detailed Description
Patients will be recruited up to the day of surgery. They will be then randomized using a computer generated table of random numbers to two groups: Group A (IV acetaminophen 1000 mg over 15 minutes at...
Eligibility Criteria
Inclusion
- Inclusion Criteria:
- Outpatient lumpectomy
- ASA I and II
- Age between 18-70
- Exclusion:
- Pregnancy
- History of liver disease
- Unable to understand the informed consent
- Chronic pain with use of opioid in the last week
- Allergy to acetaminophen
- Drop-out: surgeon or patient request
Exclusion
Key Trial Info
Start Date :
November 1 2013
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
December 1 2014
Estimated Enrollment :
70 Patients enrolled
Trial Details
Trial ID
NCT01852955
Start Date
November 1 2013
End Date
December 1 2014
Last Update
March 14 2016
Active Locations (1)
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1
Northwestern University
Chicago, Illinois, United States, 60611