Ondansetron and the QT Interval In Adult Emergency Department Patients

Ondansetron Clinical Trial

Official title:

Ondansetron and the QT Interval In Adult Emergency Department Patients

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01759420
• Other study ID #: 375393
• Status: Completed
• Phase: N/A
• First received: December 29, 2012
• Last updated: June 24, 2014
• Start date: December 2012
• Est. completion date: May 2014

Study information

• Verified date: June 2014
• Source: C.R.Darnall Army Medical Center
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Federal Government
• Study type: Observational

Clinical Trial Summary

The purpose of this study is to assess the use of the medication ondansetron (zofran) in the emergency department. There are studies of the ability of ondansetron to cause a prolongation in the QT interval (a certain measurement on an EKG) in anesthesia and cancer patients, but not on emergency department patients. This is an observational study where patients that are going to receive the anti-nausea medicine ondansetron in the emergency department will have an EKG performed every 2 minutes for 20 minutes to determine if the QT interval prolongs and returns to normal in that time period. Any serious outcomes will be reported. There is expected to be no adverse outcomes from this routinely used medication.

Description:

Intravenous ondansetron is routinely used in adult emergency department patients experiencing nausea or vomiting. The FDA has changed the drug label to warn of prolongation of the QT interval and required the manufacturer to perform additional studies. There are rare case reports of cardiac electrical toxicity to include QT prolongation, atrial fibrillation, severe bradycardia, ventricular tachycardia, supraventricular tachycardia, and the potential for Torsades de Pointes. All of the reported literature on ondansetron comes from post-operative patients, patients receiving chemotherapy, and healthy volunteers, but has never been assessed in the emergency department population. Adult emergency department patients that do not meet the exclusion criteria will be enrolled prior to receiving intravenous ondansetron. Administration of ondansetron will be at the discretion of the attending physician. A twelve-lead electrocardiogram (EKG) or 12-lead rhythm strip will be generated prior to drug administration, and every 2 minutes following drug administration for 20 minutes after administration. During the entire 20 minutes the patient will be on a cardiac monitor and if any of the defined adverse cardiac electrical events occur (non-sinus rhythm, severe bradycardia, sudden cardiac death) the patient will be treated using standard Advanced Cardiac Life Support methods and admitted for continued monitoring. The mean maximal QTc prolongation (as measured by the Bazett formula), as well as the rate of adverse cardiac events with 95% confidence intervals will be reported.

The global objective of this study is to determine if routine use of intravenous ondansetron in the emergency department is associated with cardiac risks. The primary objective is to determine the mean maximal prolongation in QTc interval from baseline as measured by the Bazett formula. The secondary objective is to determine the number of severe adverse cardiac electrical events (non-sinus rhythm, severe bradycardia, sudden cardiac death) associated with routine use of intravenous ondansetron in the adult emergency department patient.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 28
• Est. completion date: May 2014
• Est. primary completion date: May 2014
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Age >18

• Patient to receive 4mg of intravenous ondansetron

Exclusion Criteria:

• Age <18

• known long QT syndrome

• received oral or intravenous ondansetron within 4 hours of enrollment

• co-administration of any known QT prolonging agents

• QTc on baseline of >450 ms for males and >470ms for females

• allergy or known hypersensitivity to ondansetron

• altered mental status

• non-sinus rhythm on baseline EKG

• hypokalemia (as defined by the lower limit of normal for the reference laboratory)

• hypomagnesemia (as defined by the lower limit of normal for the reference laboratory)

• any presentation for chest pain with signs of ischemia on baseline EKG

• QRS duration > 120 msec

• bundle branch block (right or left)

• ventricular pre-excitation or signs of left ventricular hypertrophy with repolarization abnormalities

Study Design

Observational Model: Cohort, Time Perspective: Prospective

Related Conditions & MeSH terms

• Ondansetron

Intervention

Drug:
• Ondansetron
4mg of intravenous ondansetron

Locations

Country	Name	City	State
United States	Carl R Darnall Army Medical Center	Fort Hood	Texas
United States	Madigan Army Medical Center	Tacoma	Washington

Sponsors (2)

Lead Sponsor	Collaborator
C.R.Darnall Army Medical Center	Madigan Army Medical Center

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Change in QTc Interval With Ondansetron Administration	The primary objective is to determine the mean maximal prolongation in QTc interval from baseline as measured by the Bazett formula. A baseline EKG will be obtained and then after drug administration an EKG will be performed every 2 minutes until 20 minutes has passed. The mean maximal QTc change will be calculated.	Baseline to 20 minutes	Yes
Secondary	Number of Adverse Events	The secondary objective is to determine the number of severe adverse cardiac electrical events (non-sinus rhythm, severe bradycardia, sudden cardiac death) associated with routine use of intravenous ondansetron in the adult emergency department patient. All of these outcomes will be recorded for each patient during the emergency department stay which could range from 20 minutes to several hours.	20 minutes to 8 hours	Yes