Clinical Trials Directory

Trials / Completed

CompletedNCT03217877

Pragmatic Trial Comparing Symptom-Oriented Versus Routine Stress Testing in High-Risk Patients Undergoing Percutaneous Coronary Intervention

a Multi-center, Open-label, Nationwide Registry-based, Randomized, Pragmatic Trial Comparing 2 Post-PCI Management Strategies in High-risk PCI Patients With Complex Clinical and Lesion Characteristics

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
1,700 (actual)
Sponsor
Seung-Jung Park · Academic / Other
Sex
All
Age
20 Years
Healthy volunteers
Not accepted

Summary

The primary objective of the POST-PCI trial is to compare the clinical outcomes of a post-percutaneous coronary intervention(PCI) aggressive management strategy of routine noninvasive functional testing to a usual-care strategy of symptom-oriented functional testing in patients with high risk clinical, anatomical, and procedural characteristics who received PCI with contemporary drug-eluting stent and bioresorbable vascular scaffold.

Conditions

Interventions

TypeNameDescription
DIAGNOSTIC_TESTroutine stress testingIn the group of routine stress testing group, the preselected functional test (exercise ECG, nuclear stress testing, or stress echocardiography) will be performed at 9\~15 months after the procedure according to the practice pattern of each participating center.
DIAGNOSTIC_TESTNo Routine stress testingIn the group of symptom oriented stress testing group, the preselected functional test (exercise ECG, nuclear stress testing, or stress echocardiography) will be performed when chest pain or angina symptom is occured after the procedure according to the practice pattern of each participating center.

Timeline

Start date
2017-11-15
Primary completion
2021-10-31
Completion
2021-10-31
First posted
2017-07-14
Last updated
2022-04-05

Locations

11 sites across 1 country: South Korea

Source: ClinicalTrials.gov record NCT03217877. Inclusion in this directory is not an endorsement.