Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2026-03-26 @ 3:18 PM
Ignite Modification Date:
2026-03-26 @ 3:18 PM
NCT ID:
NCT07332494
Eligibility Criteria:
Inclusion Criteria:
1. Age 18-75 years
2. Diagnosis of Acute Coronary Syndrome (ACS) or Chronic Coronary Syndrome (CCS)
3. Status post-successful percutaneous coronary intervention (PCI).
4. Possession of a smartphone and ability to operate the application (independently or with caregiver assistance).
5. Provision of written informed consent.
Exclusion Criteria:
1. Heart Failure: NYHA Class III-IV or LVEF \< 40%.
2. Severe hepatic dysfunction (ALT/AST ≥3xULN or Total Bilirubin \>1.5 mg/dl)
3. Severe renal dysfunction (eGFR \< 30 ml/min/1.73m² or requiring dialysis)
4. Uncontrolled hypothyroidism (TSH \>1.5xULN or \>10 mIU/L, or unstable dosage within 6 weeks)
5. Life expectancy \< 1 year due to non-cardiovascular comorbidities
6. Severe sensory (hearing/vision) or cognitive impairment precluding device use
7. Conditions affecting adherence (e.g., substance use disorder, history of alcohol abuse)
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Maximum Age:
75 Years
Study:
NCT07332494
Study Brief:
Protocol Section:
NCT07332494