Health Condition 1: I708- Atherosclerosis of other arteries
Conditions
Interventions
Intervention1: NIL: NIL
Intervention2: NIL: NIL
Control Intervention1: NIL: NIL
Sponsors
Sunfox Technologies Private Limited
Eligibility
Inclusion criteria
Inclusion criteria: Patients should have symptoms such as chest pain palpitations and shortness of breath. These symptoms are indicative of potential cardiac issues and make them suitable candidates for the study and Patients referred for coronary angiography are included.
Exclusion criteria
Exclusion criteria: 1. History of Reperfusion: Patients with a history of reperfusion therapy are excluded. This criterion may be in place to focus on patients who have not undergone reperfusion and to avoid potential confounding factors related to prior treatments. 2. Pacemaker Rhythm: Patients with a pacemaker rhythm are excluded from the study. This exclusion criterion ensures that participants do not have devices that may interfere with the accurate recording and interpretation of ECG data using smartphone-based portable ECG devices.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary outcome measure is the correlation between ECG recordings obtained via smartphone-based portable ECG devices and the findings of coronary angiography. Timepoint: 6 Months | — |
Secondary
| Measure | Time frame |
|---|---|
| Secondary outcomes may include clinical outcomes (e.g., mortality rates, major adverse cardiac events), patient perspectives, and the influence of patient characteristics and confounding factors on ECG accuracy. Timepoint: 6 Months | — |
Countries
India
Contacts
Public ContactChandra Mohan Belwal
Himalayan Institute of Medical Sciences
Outcome results
None listed