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Main
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Note: This record shows only the 20 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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ClinicalTrials.gov |
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Last refreshed on:
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17 October 2012 |
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Main ID: |
NCT01498471 |
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Date of registration:
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20/12/2011 |
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Primary sponsor: |
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Public title:
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NICE Guideline 'Red Flags' to Predict Serious Outcome After Transient Loss of Consciousness
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Scientific title:
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NICE Guideline 'Red Flags' to Predict Serious Outcome After Transient Loss of Consciousness: Prospective Validation Study in the Emergency Department. |
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Date of first enrolment:
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January 2012 |
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Target sample size:
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490 |
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Recruitment status: |
Not yet recruiting |
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URL:
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http://clinicaltrials.gov/show/NCT01498471 |
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Study type:
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Observational |
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Study design:
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Observational Model: Cohort, Time Perspective: Prospective
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Countries of recruitment
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Belgium
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Contacts
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Name:
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Peter Vanbrabant, MD |
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Address:
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Telephone:
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003216343952 |
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Email:
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peter.vanbrabant@uzleuven.be |
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Affiliation:
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- Adult patients (>= 16 years) with a complaint of TLoC
Exclusion Criteria:
- Patients needing immediate treatment, with trauma related or drug or alcohol related
TLoC were excluded, as well as patient with persistent altered level of
consciousness, simple fall and drop attack
Age minimum:
16 Years
Age maximum:
N/A
Gender:
Both
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Health Condition(s) or Problem(s) studied
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Syncope
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Primary Outcome(s)
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serious outcome
[Time Frame: day 7]
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Secondary Outcome(s)
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serious outcome
[Time Frame: 1 year]
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Secondary ID(s)
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UZ/PVB/2011
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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