NCT01201993SuspendedNot Applicable
Observational Study Following After Patients Admitted With Syncope
Carmel Medical Center1 site in 1 country40 target enrollmentStarted: August 2010Last updated:
Conditions
Trial Snapshot
- Phase
- Not Applicable
- Status
- Suspended
- Sponsor
- Enrollment
- 40
- Locations
- 1
- Primary Endpoint
- diagnosis
Study Overview
Brief Summary
The investigators hypothesis is that a significant number of patients may remain without specific cause and have recurrent syncope with its associated physical and mental morbidity.
Detailed Description
-
Patients with diagnosis of syncope who were admitted to the medical ward will be interviewed and their charts reviewed to rule in or out the diagnosis of syncope.
-
Assess physical and mental injury as a result of syncope.
-
The lab workup will be documented including;
-
- Routine blood tests.
- troponin level.
-
- ECG.
- Echocardiogram
- Brain CT.
- EEG.
- U/S doppler of carotids.
- Tilt tests.
- At the time of diagnosis the final diagnosis will be documented including recommendations for patients to prevent syncope after discharge.
- Follow up after patients by phone verifying recurrence of syncope and resulting physical and or mental injury if any.
Study Design
- Study Type
- Observational
- Observational Model
- Case Only
- Time Perspective
- Prospective
Eligibility Criteria
- Ages
- 18 Years to — (Adult, Older Adult)
- Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- •patients with diagnosis of syncope on admission to the medical ward.
Exclusion Criteria
- •patients with loss of consciousness due to other than low perfusion of the brain
- •patients that can't sign a consent form
- •patients that we can't get details about the episode of the syncope
Outcomes
Primary Outcomes
diagnosis
Time Frame: 1 year
Final diagnosis as a cause of syncope
Secondary Outcomes
- recurrence(6 months)
- physical injury(6 months)
- Mental effect(6 months)
Investigators
Study Sites (1)
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