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Digital Home-Based Management to Improve Rehabilitation Outcomes in Patients After Day-Case Coronary Stenting

A Single-Center Randomized Controlled Clinical Trial of Digital Out-of-Hospital Clinical Management to Improve Clinical Prognosis in Patients Undergoing Day-Case Coronary Stenting

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600129057
Enrollment
Unknown
Registered
2026-07-29
Start date
2026-08-01
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Coronary artery disease

Interventions

Intervention group:The patients in the experimental group were comprehensively managed using the digital clinical management system independently developed by Chengdu Harriet Medical Technology Co., L
Control group:Without using a digital clinical management system, only the routine post-hospital management after coronary heart disease day-case stent surgery is adopted, which includes routine healt

Sponsors

Northern Jiangsu People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1.Aged between 18 and 65 years inclusive; 2.Diagnosed with coronary artery disease; 3.Underwent day-case stent implantation; 4.Subjects were willing to comply with the study protocol and provided written informed consent.

Exclusion criteria

Exclusion criteria: 1.Patients with planned revascularization within one year; 2.Pregnant or breastfeeding patients, or those planning to become pregnant within one year; 3.Patients with a medical history of non-ischemic cardiomyopathy, including viral myocarditis, dilated cardiomyopathy, hypertrophic cardiomyopathy, peripartum cardiomyopathy, etc; 4.Patients with moderate or severe valvular heart disease or a history of valve replacement; 5.Severe liver dysfunction (ALT >= 3 times the upper limit of normal) or renal dysfunction (eGFR < 60 mL/min/1.73 m^2); 6.Patients complicated with malignant tumors or other diseases with an expected survival time of less than 1 year;

Design outcomes

Primary

MeasureTime frame
Cumulative incidence of MACE;

Secondary

MeasureTime frame
The incidence rate of MACE events (including all-cause death, myocardial infarction, and stroke);Cardiovascular death;Psychogenic readmission;Bleeding incidence rate (BARC classification);Quality of life;Blood pressure, heart rate, blood lipid, and blood sugar compliance rates;

Countries

China

Contacts

Public ContactXu Bing

Northern Jiangsu People's Hospital

nyxb1980@163.com+86 514 87373262

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Aug 10, 2026