Clinical Trials Directory

Trials / Completed

CompletedNCT01069536

Efficacy and Akathisia Incidence of Slow Infusion Metoclopramide

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
140 (actual)
Sponsor
Pamukkale University · Academic / Other
Sex
All
Age
18 Years – 65 Years
Healthy volunteers
Not accepted

Summary

Study Objective: The purpose of this study is to compare the effects of metoclopramide administration in bolus versus slow infusion medications in ED patients complaining of nausea for the determination of the therapeutic effect and prevention of akathisia. Methods: This was a prospective, randomized, double-blind trial. The investigation was held between 01 March 2007 and 01 May 2008, in the Emergency Department of Pamukkale University Faculty of Medicine. The patients with moderate to severe nausea randomized and divided into two groups as for the previously planned administration type of drug. Ten mg metoclopramide was administered in one group with slow infusion (SIG) in 15 minutes, via 2 minutes bolus infusion (BIG) into the other group. Whole procedure was observed, akathisia and nausea scores and vital changes were recorded.

Conditions

Interventions

TypeNameDescription
DRUGmetoclopramide 10 mg

Timeline

Start date
2007-03-01
Primary completion
2007-03-01
Completion
2008-05-01
First posted
2010-02-17
Last updated
2010-02-17

Source: ClinicalTrials.gov record NCT01069536. Inclusion in this directory is not an endorsement.

Efficacy and Akathisia Incidence of Slow Infusion Metoclopramide (NCT01069536) · Clinical Trials Directory