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IV Acetaminophen for Postoperative Analgesia

NCT01798316 · Status: TERMINATED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 105

Last updated 2017-05-31

Study results available
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Summary

The purpose of this study is to evaluate the use of IV acetaminophen for postoperative pain management after laparoscopic cholecystectomy to determine if its use to supplement standard of care pain management decreases the incidence of post-operative nausea and vomiting.

Conditions

  • Postoperative Pain
  • Postoperative Nausea
  • Postoperative Vomiting

Interventions

DRUG

IV Acetaminophen

Single dose, 1000g mg infusion over 15 minutes plus standard of care pain management regimen

DRUG

Standard of Care

Standard of care pain management regimen, no IV Acetaminophen,

Sponsors & Collaborators

  • Northwell Health

    lead OTHER

Principal Investigators

  • Frank J Overdyk, MD · Northwell Health

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2013-03-31
Primary Completion
2015-09-30
Completion
2015-09-30

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01798316 on ClinicalTrials.gov