Expired Study
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New York, New York 10025


Purpose:

The investigators want to look at how patients admitted after passing out (syncope) or nearly passing out (pre-syncope) do after going home and how many of them remain free of symptoms of syncope or pre-syncope.


Criteria:

Inclusion Criteria: - All adult patients (age 18 or older) admitted with syncope or near-syncope Exclusion Criteria: - Patients who do not speak/read the language of the consent form - Prisoners - Patients who are of altered mental status or had head trauma - Refusal or inability to sign consent


Study is Available At:


Original ID:

ESTOP-08-024


NCT ID:

NCT00764985


Secondary ID:


Study Acronym:

E-STOP


Brief Title:

Evaluation of Syncope,Its Diagnosis, Treatment, Outcome and Prognosis


Official Title:

E-STOP Registry: A Registry for the Evaluation of Syncope,Its Diagnosis, Treatment, Outcome and Prognosis Using Our SELF-Pathway


Overall Status:

Completed


Study Phase:

N/A


Genders:

Both


Minimum Age:

18 Years


Maximum Age:

N/A


Quick Facts

Healthy Volunteers
Oversight Has DMC
Study Is FDA Regulated
Study Is Section 801
Has Expanded Access

Study Source:

St. Luke's-Roosevelt Hospital Center


Oversight Authority:

United States: Institutional Review Board


Reasons Why Stopped:


Study Type:

Observational


Study Design:

Observational Model: Cohort, Time Perspective: P


Number of Arms:

0


Number of Groups:

1


Total Enrollment:

540


Enrollment Type:

Anticipated


Study Dates

Start Date:June 2008
Completion Date:July 2010
Completion Type:Actual
Primary Completion Date:July 2009
Primary Completion Type:Actual
Verification Date:July 2010
Last Changed Date:July 1, 2010
First Received Date:October 1, 2008

Study Outcomes

There are no available Study Outcomes

Study Interventions

There are no available Study Interventions

Study Arms

Study Arm Type:Other
Arm Name:Syncope

Study Agencies

Agency Class:Other
Agency Type:Lead Sponsor
Agency Name:St. Luke's-Roosevelt Hospital Center
Agency Class:Industry
Agency Type:Collaborator
Agency Name:Transoma Medical

Samples and Retentions

Study Population: All patietns admitted to the adult medicine service at St. Luke's-Roosevelt Hospital with diagnossi of syncope or near syncope
Sample Method:Non-Probability Sample

Study References

There are no available Study References

Data Source: ClinicalTrials.gov

Date Processed: January 21, 2020

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