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Exercise rehabilitation study of patients with angina pectoris after PCI under the guidance of radionuclide myocardial perfusion: a randomized controlled trial

Exercise rehabilitation study of patients with angina pectoris after PCI under the guidance of radionuclide myocardial perfusion: a randomized controlled trial

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200065131
Enrollment
Unknown
Registered
2022-10-28
Start date
2022-10-31
Completion date
Unknown
Last updated
2023-05-15

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

Conditions

Angina pectoris after PCI

Interventions

one:traditional exercise rehabilitation exercise
two:new grouping exercise rehabilitation exercise

Sponsors

The Sixth Medical Center of PLA General Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: (1) PCI with residual stenosis<50%; (2) Symptoms of angina after PCI were found. Angina pectoris was diagnosed according to the national health industry standard Diagnostic Standard for Coronary Atherosclerotic Heart Disease (WS 319-2010); (3) Age 18-70 years old, regardless of gender; (4) The patient voluntarily participated in the study and signed the informed consent form.

Exclusion criteria

Exclusion criteria: (1) Angina pectoris caused by non PCI surgery (2) unstable condition after acute myocardial infarction with myocardial ischemia (3) high-risk unstable angina pectoris with elevated markers of myocardial injury (4) tachyarrhythmia or bradyarrhythmia (such as ventricular tachycardia, sick sinus syndrome, atrioventricular block of more than two degrees, left bundle branch block, etc.) that causes discomfort and accompanied by abnormal hemodynamics (5) severe left trunk stenosis Aortic valve stenosis, acute aortic dissection, severe pulmonary hypertension, obstructive hypertrophic cardiomyopathy (6) decompensated heart failure, severe left ventricular dysfunction (LVEF200/110 mmHg), Obvious hypotension (1.5 mg/dL) Patients with tumor and other diseases (13) can not tolerate or are allergic to related developer (14) have serious artifacts, poor image quality (15) do not cooperate with and reject the researcher, such as severe psychiatric diseases, and SCL-90 scores = 60.

Design outcomes

Primary

MeasureTime frame
summed stress score;summed rest score;summed difference score;

Countries

CHINA

Contacts

Public ContactChuang Zhang

The Sixth Medical Center of Chinese People's Liberation Army General Hospital

13910896236@163.com13910896236

Outcome results

None listed

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