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
| Type | Name | Description |
|---|---|---|
| DRUG | metoclopramide 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.