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Syncope algorithms in the emergency department with structured follow-up. How effective is a standardised approach at improving diagnostic yield, quality of life and decreasing health care costs? The SYNERGY study

Recruiting
Conditions
syncope
fainting
Registration Number
NL-OMON45663
Lead Sponsor
eids Universitair Medisch Centrum
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Not specified
Target Recruitment
550
Inclusion Criteria

All patients at the emergency department because of suspected syncope

Exclusion Criteria

(1) Those aged <18 years
(2) Those in whom a serious life threatening condition is identified in the ED (massive bleeding, pulmonary embolus)
(3) Those who attended any ED because of syncope in the previous year
(4) Those with a learning disability
(5) Those presenting with presyncope
(6) Those who already attented a tertiary syncope clinic

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
<p>Proportion of patients with an accurate diagnosis (as determined by an expert<br /><br>panel at 1 year follow-up)</p><br>
Secondary Outcome Measures
NameTimeMethod
<p>Number of admissions because of syncope, time to diagnosis following ED<br /><br>presentation, syncope recurrence, Healthcare and societal costs within 1 year<br /><br>following ED presentation, number of syncope-related tests and consultations,<br /><br>QoL</p><br>
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