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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01792544
Other study ID # SUIRB-021780
Secondary ID
Status Completed
Phase N/A
First received February 12, 2013
Last updated April 26, 2016
Start date July 2011
Est. completion date July 2015

Study information

Verified date April 2016
Source VA Palo Alto Health Care System
Contact n/a
Is FDA regulated No
Health authority United States: Federal Government
Study type Interventional

Clinical Trial Summary

This study examines the impact of adding a statement to the echocardiography report that advises anyone reading the report regarding if and when a follow-up study is recommended.


Recruitment information / eligibility

Status Completed
Enrollment 1706
Est. completion date July 2015
Est. primary completion date November 2013
Accepts healthy volunteers No
Gender Both
Age group N/A and older
Eligibility Inclusion Criteria:

All patients undergoing echocardiography where the physician creating the report feels a comment is appropriate regarding when follow-up should or should not occur.

Exclusion Criteria:

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Health Services Research


Related Conditions & MeSH terms


Intervention

Other:
Statement

No Statement


Locations

Country Name City State
United States VA Palo Alto HCS Palo Alto California

Sponsors (1)

Lead Sponsor Collaborator
VA Palo Alto Health Care System

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Inappropriate follow-up Performance of a follow-up echocardiogram when it was not indicated or not performing for a follow-up echocardiogram when it was indicated. 1 year No
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