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Comparison of different scoring methods [ROSE, FAINT, CSRS] to predict short-term health risks in adults with a transient loss of consciousness and visit the Emergency Department. A follow-up call after 30 days will be made to check their health.

Comparative evaluation of risk stratification scores for predicting short-term adverse events in adult patients presenting with syncope to the Emergency Department. - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2024/10/075196
Enrollment
114
Registered
2024-10-14
Start date
Unknown
Completion date
Unknown
Last updated
2024-11-11

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

Conditions

Health Condition 1: R55- Syncope and collapse

Interventions

Intervention1: NIL: NIL

Sponsors

Department of Emergency Medicine
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Individuals aged above 18 presenting with syncope to the Emergency Department and consenting for the study are included.

Exclusion criteria

Exclusion criteria: individuals under 18 years of age, pregnant individuals, those unable to provide written consent, Individuals diagnosed with causes other than syncope for loss of consciousness (e.g: hypoglycemia, seizure, poisoning, suspected intoxication and head trauma)

Design outcomes

Primary

MeasureTime frame
Mortality Outcome will be assessed at the end of 4 weeksTimepoint: Mortality will be assessed at the end of 4 weeks—

Secondary

MeasureTime frame
1. Acute Coronary Syndrome/Myocardial Infarction 2. Cerebrovascular Accident 3. Pulmonary Embolism Outcome will be assessed at the end of 4 weeks(30 days)Timepoint: Outcomes will be assessed at the end of 4 weeks—

Countries

India

Contacts

Public ContactDr Vimal Krishnan S

Kasturba Medical College, Manipal

vimal.krishnan@manipal.edu7907953222

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026