Clinical Reminders in Test Reports to Improve Guideline Compliance

This study has been completed.
Sponsor:
Information provided by (Responsible Party):
Department of Veterans Affairs
ClinicalTrials.gov Identifier:
NCT00414401
First received: December 19, 2006
Last updated: August 1, 2012
Last verified: December 2006

December 19, 2006
August 1, 2012
May 2001
Not Provided
Prescription for any beta-blocker [ Designated as safety issue: No ]
Prescription for any beta-blocker
Complete list of historical versions of study NCT00414401 on ClinicalTrials.gov Archive Site
Prescription for carvedilol or metoprolol succinate [ Designated as safety issue: No ]
Prescription for carvedilol or metoprolol succinate
Not Provided
Not Provided
 
Clinical Reminders in Test Reports to Improve Guideline Compliance
Clinical Reminders in Test Reports to Improve Guideline Compliance

Although beta-blockers are known to prolong survival for patients with reduced left ventricular ejection fraction, their use in the community and the VA is suboptimal.

Background:

Although beta-blockers are known to prolong survival for patients with reduced left ventricular ejection fraction, their use in the community and the VA is suboptimal.

Objectives:

To determine if a reminder attached to the echocardiography report would increase the use of beta-blockers among patients with depressed left ventricular function.

Methods:

We are randomizing consecutive patients undergoing echocardiography at one of three VA echocardiography laboratories with reduced left ventricular ejection fraction (<40%) and no echocardiographic contraindication to beta-blockers (e.g. aortic stenosis) to a reminder for use of beta-blockers or to no reminder. The reminder gives starting doses for two commonly used beta-blockers (carvedilol and metoprolol). Patients are excluded from the analysis if they leave the health care system or die within three months of randomization. The primary outcome is a prescription for a beta-blocker between three and nine months following echocardiography

Status:

The project is complete.

Interventional
Not Provided
Allocation: Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Parallel Assignment
Masking: Open Label
Heart Failure, Congestive
Behavioral: Clinical Reminder
Arm 1
Intervention: Behavioral: Clinical Reminder

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
1500
June 2006
Not Provided

Inclusion Criteria:

Those undergoing echocardiography at one of the participating laboratories with an ejection fraction < 45%.

Exclusion Criteria:

aortic stenosis, mitral stenosis

Both
18 Years and older
No
Contact information is only displayed when the study is recruiting subjects
United States
 
NCT00414401
IIR 01-108
No
Department of Veterans Affairs
Department of Veterans Affairs
Not Provided
Principal Investigator: Paul A. Heidenreich, MD VA Palo Alto Health Care System
Department of Veterans Affairs
December 2006

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP