Trial record 16 of 180 for:    Syncope

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
  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.


Condition
Syncope

Study Type: Observational
Study Design: Observational Model: Cohort
Time Perspective: Prospective
Official Title: E-STOP Registry: A Registry for the Evaluation of Syncope,Its Diagnosis, Treatment, Outcome and Prognosis Using Our SELF-Pathway

Resource links provided by NLM:


Further study details as provided by St. Luke's-Roosevelt Hospital Center:

Estimated Enrollment: 540
Study Start Date: June 2008
Study Completion Date: July 2010
Primary Completion Date: July 2009 (Final data collection date for primary outcome measure)

  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
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

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
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00764985

Locations
United States, New York
St. Luke's-Roosevelt Hospital Center
New York, New York, United States, 10025
Sponsors and Collaborators
St. Luke's-Roosevelt Hospital Center
Transoma Medical
  More Information

No publications provided

Responsible Party: Suneet Mittal, St. Luke's-Roosevelt Hospitals
ClinicalTrials.gov Identifier: NCT00764985     History of Changes
Other Study ID Numbers: ESTOP-08-024
Study First Received: October 1, 2008
Last Updated: July 1, 2010
Health Authority: United States: Institutional Review Board

Keywords provided by St. Luke's-Roosevelt Hospital Center:
Syncope
Pre-Syncope
Fainting

Additional relevant MeSH terms:
Syncope
Unconsciousness
Consciousness Disorders
Neurobehavioral Manifestations
Neurologic Manifestations
Nervous System Diseases
Signs and Symptoms

ClinicalTrials.gov processed this record on April 15, 2014