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Droperidol Versus Metoclopramide for the Treatment of Primary Headaches in the Emergency Department: A Prospective Randomized, Double-blinded Trial.

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City:   Iowa City
State:   Iowa
Zip Code:   52242
Conditions:   Primary Headaches (Includes Migraines, Tension, Cluster Headaches)
Purpose:   The purpose of this study is to determine if droperidol is equally as effective as metoclopramide for treatment of primary headaches in the Emergency Department.
Study Summary:  
Criteria:   Inclusion Criteria: - 18 years old to 65 years old, diagnosis of primary headache Exclusion Criteria: - Allergy to study medications, pregnant, breast-feeding, prisoners, non-english speaking, not eligible to receive droperidol based on ED protocol (see below), patients in whom head trauma, infection, vascular disorders, and disorders of facial or cranial structures are suspected ED Droperidol Protocol Droperidol must NOT be used in patients with any of the following: - Known or suspected QT prolongation, including congenital long QT syndrome - Cardiac Disease [cardiomyopathy, congestive heart failure, hypertension, ischemic heart disease, myocardial infarction, bradycardia (< 50 bpm)] - History of the following: - Renal failure - Cerebrovascular disease - Diabetes or hypoglycemia - Alcoholism/alcohol abuse - Pituitary insufficiency - Hypothyroidism - Hypothermia - Anorexia - Advanced age (>65 yrs) - Use of the following medications: digoxin, benzodiazepine, diuretics, IV opiates, or other medications known to prolong the QTc interval.
NCT ID:   NCT01406860
Primary Contact:   Principal Investigator
Jon Van Heukelom, MD
University of Iowa

Backup Contact:   N/A
Location Contact:   Iowa City, Iowa 52242
United States



There is no listed contact information for this specific location.

Site Status: N/A

Data Source:   ClinicalTrials.gov
Date Processed:   May 23, 2013
Modifications to this listing:   Only selected fields are shown, please use the link below to view all information about this clinical trial.
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