Evaluation of Syncope,Its Diagnosis, Treatment, Outcome and Prognosis (E-STOP)

This study has been completed.

Sponsor:

Collaborator:

Transoma Medical

Information provided by:

St. Luke's-Roosevelt Hospital Center

ClinicalTrials.gov Identifier:

NCT00764985

First received: October 1, 2008

Last updated: July 1, 2010

Last verified: July 2010

History of Changes

Tracking Information
First Received Date ^ICMJE	October 1, 2008
Last Updated Date	July 1, 2010
Start Date ^ICMJE	June 2008
Primary Completion Date	July 2009 (final data collection date for primary outcome measure)
Current Primary Outcome Measures ^ICMJE	Not Provided
Original Primary Outcome Measures ^ICMJE	Not Provided
Change History	Complete list of historical versions of study NCT00764985 on ClinicalTrials.gov Archive Site
Current Secondary Outcome Measures ^ICMJE	Not Provided
Original Secondary Outcome Measures ^ICMJE	Not Provided
Current Other Outcome Measures ^ICMJE	Not Provided
Original Other Outcome Measures ^ICMJE	Not Provided

Descriptive Information
Brief Title ^ICMJE	Evaluation of Syncope,Its Diagnosis, Treatment, Outcome and Prognosis
Official Title ^ICMJE	E-STOP Registry: A Registry for the Evaluation of Syncope,Its Diagnosis, Treatment, Outcome and Prognosis Using Our SELF-Pathway
Brief Summary	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.
Detailed Description	Not Provided
Study Type ^ICMJE	Observational
Study Design ^ICMJE	Observational Model: Cohort Time Perspective: Prospective
Target Follow-Up Duration	Not Provided
Biospecimen	Not Provided
Sampling Method	Non-Probability Sample
Study Population	All patietns admitted to the adult medicine service at St. Luke's-Roosevelt Hospital with diagnossi of syncope or near syncope
Condition ^ICMJE	Syncope
Intervention ^ICMJE	Not Provided
Study Group/Cohort (s)	Syncope
Publications *	Not Provided
* Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.

Recruitment Information
Recruitment Status ^ICMJE	Completed
Estimated Enrollment ^ICMJE	540
Completion Date	July 2010
Primary Completion Date	July 2009 (final data collection date for primary outcome measure)
Eligibility Criteria ^ICMJE	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
Gender	Both
Ages	18 Years and older
Accepts Healthy Volunteers	No
Contacts ^ICMJE	Contact information is only displayed when the study is recruiting subjects
Location Countries ^ICMJE	United States

Administrative Information
NCT Number ^ICMJE	NCT00764985
Other Study ID Numbers ^ICMJE	ESTOP-08-024
Has Data Monitoring Committee	No
Responsible Party	Suneet Mittal, St. Luke's-Roosevelt Hospitals
Study Sponsor ^ICMJE	St. Luke's-Roosevelt Hospital Center
Collaborators ^ICMJE	Transoma Medical
Investigators ^ICMJE	Not Provided
Information Provided By	St. Luke's-Roosevelt Hospital Center
Verification Date	July 2010
^ICMJE Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP

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