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A study of the trajectory of intrinsic capacity in middle-aged and elderly patients after percutaneous coronary intervention and its impact on unplanned readmissions

A study of the trajectory of intrinsic capacity in middle-aged and elderly patients after percutaneous coronary intervention and its impact on unplanned readmissions

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400087129
Enrollment
Unknown
Registered
2024-07-22
Start date
2024-07-23
Completion date
Unknown
Last updated
2024-07-29

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

Conditions

Percutaneous coronary intervention

Interventions

Middle-aged and elderly patients after percutaneous coronary intervention:None

Sponsors

The Second Affiliated Hospital of Zhejiang University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
45 Years to 100 Years

Inclusion criteria

Inclusion criteria: ? Age = 45 years old; ? Patients undergoing emergency or elective PCI treatment; ? Conscious, able to communicate normally and able to complete physical assessment tests; ? Those who signed the informed consent and were willing to accept and complete the whole study.

Exclusion criteria

Exclusion criteria: ? Those who have cardiogenic shock and severe infection at the time of admission; ? Those who are combined with other organs failure such as liver and kidney; ? Patients with terminal illnesses with a life expectancy of 6 months; ? People with mental illness, cognitive impairment, Alzheimer's disease or other dementia, critically ill patients, pregnant women, people with disabilities and other vulnerable groups.

Design outcomes

Primary

MeasureTime frame
Intrinsic capacity;Unplanned readmission;

Secondary

MeasureTime frame
General demographic information;

Countries

China

Contacts

Public ContactLeiwen Tang

The Second Affiliated Hospital of Zhejiang University School of Medicine

tanglw@zju.edu.cn+86 134 5697 0742

Outcome results

None listed

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