CClinicalTrials.gg
Active, not recruitingNCT07465692Updated Mar 12, 2026

Long-term Results of Rehabilitation of Patients With Myocardial Infarction After Coronary Artery Stenting. The Register.

An interventional study of Physical training program in Myocardial Infarction, sponsored by National Medical Research Center for Therapy and Preventive Medicine. Active, not recruiting. Open to participants aged 18 Years to 75 Years. Per ClinicalTrials.gov, last updated 2026-03-12.

Sponsored by National Medical Research Center for Therapy and Preventive Medicine · Not applicable, Interventional, and Prevention

From the registry’s dates

  • Registered 12 years 9 months after the study started (first participant enrolled Jun 2013, registered Mar 2026).
Phase
Not applicable
Study type
Interventional
Enrollment
1,046
Allocation
Randomized
Ages
18 Years to 75 Years
Sex
All
01

Study summary

Endovascular intervention is one of the most effective treatment for acute coronary syndrome. Therefore, studying the impact of various medical rehabilitation programs on the course of coronary heart disease, patient quality of life, restenosis, and prognosis is of scientific and practical interest. Medical rehabilitation is a crucial stage in patient care after myocardial revascularization. Regular moderate-intensity physical activity helps improve endothelial function and has anti-inflammatory and antithrombogenic effects. Improving a patient's prognosis after myocardial infarction depends on the duration and intensity of cardiac rehabilitation programs, as well as the patient's motivation. Therefore, this issue requires further study, particularly in patients who have undergone endovascular interventions on coronary arteries.

Read the detailed description

The study was an interventional (clinical) trial, randomized in parallel groups. A total of 1,046 patients were included.

A total of 1,046 patients of both sexes were randomized into two groups. Group 1 (control) patients received standard therapy required for patients undergoing coronary artery stenting during the acute phase of myocardial infarction. They continued their usual physical activity and attended a school for patients with myocardial infarction. Group 2 patients received standard therapy required for patients undergoing coronary artery stenting during the acute phase of myocardial infarction, attended a school for patients with myocardial infarction, and participated in a physical training program. The training program lasted over four months. Postoperatively, patients underwent blood tests, echocardiography, ECG, and bicycle ergometry. The next visit was performed after an average of eight years (with a maximum follow-up period of 11 years). Cardiovascular events were assessed at this stage. Patients who were unable to attend the clinic were interviewed by telephone.

02

Conditions studied

  • Myocardial Infarction

Keywords

  • myocardial infarction
  • rehabilitation
  • coronary artery stenting
03

In context

Myocardial Infarction

2,744 studies on the registry are indexed under Myocardial Infarction; 418 are open to participants now.

This study's enrollment of 1,046 is above the median of 148 across 1,595 interventional studies indexed under Myocardial Infarction.

Browse Myocardial Infarction studies →

Lead sponsor

National Medical Research Center for Therapy and Preventive Medicine is the lead sponsor of 28 studies on the registry; 10 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 75 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Acute myocardial infarction, coronary artery stenting

Exclusion criteria

Exclusion Criteria:

  • Age (younger 18 years, older 75 years)
05

Study design

Phase
Not applicable
Primary purpose
Prevention
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
1,046 participants (actual)

Study arms

  • Experimental
    Physical training

    Integrated Rehabilitation consisting of exercise training and school for patients

    Other: Physical training program

  • No intervention
    Control

    Standard follow-up and attending school for patients at the participating heart center

Interventions

  • OtherPhysical training program

    Integrated Rehabilitation consisting of exercise training for at least 1.5 months

06

What researchers measure

Primary outcomes

  1. Combined

    Cardiovascular mortality, non-fatal acute myocardial infarction, non-fatal stroke, need for revascularization

    Time frame: 20 years

Secondary outcomes

  1. All-cause mortality

    Time frame: 20 years

  2. Composite endpoint of major adverse cardiovascular events (MACE)

    Composite endpoint of major adverse cardiovascular events (MACE), defined as the first occurrence of any of the following: recurrent myocardial infarction, ischemic or hemorrhagic stroke, repeat coronary revascularization (PCI or CABG), cardiovascular death.

    Time frame: 20 years

  3. cardiovascular mortality

    Time frame: 20 years

  4. myocardial infarction

    Time frame: 20 years

  5. stroke

    Time frame: 20 years

  6. need for revascularization

    Time frame: 20 years

  7. hospitalization due to cardiovascular complications

    Time frame: 20 years

07

Study locations

No study locations are listed for this record.

08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Mar 12, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT07465692
Lead sponsor
National Medical Research Center for Therapy and Preventive Medicine
Responsible party
Sponsor
First posted
Mar 12, 2026
Start date
Jun 2013
Primary completion
Dec 2026 (estimated)
Completion
Dec 2026 (estimated)
Last update
Mar 12, 2026

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is active, not recruiting, as verified in Mar 2026. You cannot join it, but the record below documents what was studied.

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