NCT02046382View on ClinicalTrials.gov

RCT (Randomized Controlled Trial) of IV Acetaminophen for Post Cesarean Pain Relief

PHASE4CompletedINTERVENTIONAL
Enrollment

132

Participants

Timeline

Start Date

January 31, 2014

Primary Completion Date

December 31, 2016

Study Completion Date

May 31, 2017

Conditions
Cesarean SectionPain, Postoperative
Interventions
DRUG

IV Acetaminophen

1000mg dose of IV acetaminophen in 100mL solution every 8 hours for 48 hours. The first dose will be administered intraoperatively following delivery of the baby. A total of 6 doses will be given.

DRUG

Placebo

100 mL of Normal Saline every 8 hours for 48 hours. The first does will be administered intraoperatively following delivery of the baby. A total of 6 doses will be given.

Trial Locations (1)

45220

TriHealth Good Samaritan Hospital, Cincinnati

All Listed Sponsors
lead

TriHealth Inc.

OTHER

NCT02046382 - RCT (Randomized Controlled Trial) of IV Acetaminophen for Post Cesarean Pain Relief | Biotech Hunter | Biotech Hunter