Establishing the Link Between Spandan Smartphone ECG and Angiography in STEMI patient Diagnosis
- Conditions
- Health Condition 1: I708- Atherosclerosis of other arteries
- Registration Number
- CTRI/2024/07/071055
- Lead Sponsor
- Sunfox Technologies Private Limited
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 80
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.
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.
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The primary outcome measure is the correlation between ECG recordings obtained via smartphone-based portable ECG devices and the findings of coronary angiography. <br/ ><br>Timepoint: 6 Months
- Secondary Outcome Measures
Name Time Method 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. <br/ ><br>Timepoint: 6 Months