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CompletedNCT00764985E-STOPUpdated Jul 2, 2010

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

An observational study in Syncope, sponsored by St. Luke's-Roosevelt Hospital Center. Completed at 1 site in United States. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2010-07-02.

Sponsored by St. Luke's-Roosevelt Hospital Center · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
540
Ages
18 Years and older
Sex
All
01

Study 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.

02

Conditions studied

  • Syncope

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Keywords

  • Syncope
  • Pre-Syncope
  • Fainting
03

In context

Syncope

232 studies on the registry are indexed under Syncope; 45 are open to participants now.

This study's planned enrollment of 540 is above the median of 235 across 95 observational studies indexed under Syncope.

Browse Syncope studies →

Lead sponsor

St. Luke's-Roosevelt Hospital Center is the lead sponsor of 69 studies on the registry; none are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
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

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • All adult patients (age 18 or older) admitted with syncope or near-syncope

Exclusion criteria

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
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
540 participants (estimated)

Groups and cohorts

  • Syncope
06

Study locations

1 site
  • St. Luke's-Roosevelt Hospital Center
    New York, New York 10025, United States
07

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 2, 2010, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
08

Registry details

Key details

Study ID
NCT00764985
Lead sponsor
St. Luke's-Roosevelt Hospital Center
Collaborators
Transoma Medical
First posted
Oct 2, 2008
Start date
Jun 2008
Primary completion
Jul 2009
Completion
Jul 2010
Last update
Jul 2, 2010

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Jul 2010. You cannot join it, but the record below documents what was studied.

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Discussion

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