NCT01460667View on ClinicalTrials.gov

Efficacy of IV Acetaminophen in Acute Post-Operative Pain Control in Laparoscopic Roux-en-Y Gastric Bypass Surgery (LRYGBP) Patients

NAUnknownINTERVENTIONAL
Enrollment

85

Participants

Timeline

Start Date

October 31, 2011

Primary Completion Date

October 31, 2012

Conditions
Morbid Obesity
Interventions
DRUG

IV acetaminophen

IV acetaminophen 1000 mg (100 mL) every 6 hours over 30 hours

DRUG

IV normal saline

0.9% normal saline IV, every 6 hours over 30 hours.

Trial Locations (1)

48532

RECRUITING

McLaren Regional Medical Center, Flint

Sponsors

Collaborators (1)

Cadence Pharmaceuticals
All Listed Sponsors
collaborator

Cadence Pharmaceuticals

INDUSTRY

lead

McLaren Regional Medical Center

OTHER

NCT01460667 - Efficacy of IV Acetaminophen in Acute Post-Operative Pain Control in Laparoscopic Roux-en-Y Gastric Bypass Surgery (LRYGBP) Patients | Biotech Hunter | Biotech Hunter