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

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

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00764985
Acronym
E-STOP
Enrollment
540
Registered
2008-10-02
Start date
2008-06-30
Completion date
2010-07-31
Last updated
2010-07-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Syncope

Keywords

Syncope, Pre-Syncope, Fainting

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.

Interventions

None listed

Sponsors

Transoma Medical
CollaboratorINDUSTRY
St. Luke's-Roosevelt Hospital Center
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026