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Comparing Intravenous and Oral Paracetamol for Cholecystectomy

NCT00292214 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 30

Last updated 2007-03-09

No results posted yet for this study

Summary

To determine the amount of paracetamol in the blood when given in either intravenous or oral forms prior to cholecystectomy. The clinical effectiveness of each form will also be evaluated with pain scores and the use of other pain relief drugs.

Conditions

  • Laparoscopic Cholecystectomy

Interventions

DRUG

Paracetamol (acetaminophen)

Sponsors & Collaborators

  • Melbourne Health

    lead OTHER

Principal Investigators

  • Malcolm Hogg, Anaesthetist · Melbourne Health

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

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

Timeline & Regulatory

Start
2005-10-31
Completion
2006-10-31

Countries

  • Australia

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 NCT00292214 on ClinicalTrials.gov