NCT01852955View on ClinicalTrials.gov

Perioperative Systemic Acetaminophen to Improve Postoperative Quality of Recovery After Ambulatory Breast Surgery

NACompletedINTERVENTIONAL
Enrollment

70

Participants

Timeline

Start Date

November 30, 2013

Primary Completion Date

December 31, 2014

Study Completion Date

December 31, 2014

Conditions
Pain
Interventions
DRUG

IV acetaminophen

Administration of IV acetaminophen 1000 mg over 15 minutes at the start of surgical closure

DRUG

Placebo

Administration of placebo (sterile normal saline)group-same volume of saline solution administered in the same fashion as the acetaminophen

Trial Locations (1)

60611

Northwestern University, Chicago

All Listed Sponsors
lead

Northwestern University

OTHER

NCT01852955 - Perioperative Systemic Acetaminophen to Improve Postoperative Quality of Recovery After Ambulatory Breast Surgery | Biotech Hunter | Biotech Hunter