Skip to content

Clinical comparative study of different starting time and application methods of cardiac rehabilitation after coronary artery bypass grafting

Clinical comparative study of different starting time and application methods of cardiac rehabilitation after coronary artery bypass grafting

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800016743
Enrollment
Unknown
Registered
2018-06-21
Start date
2018-06-20
Completion date
Unknown
Last updated
2018-06-25

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

Conditions

Coronary atherosclerotic heart disease

Interventions

Early postoperative cardiac rehabilitation intervention group:Early postoperative cardiac rehabilitation intervention group
The rehabilitation group was started at 1~2 months after operation:The rehabilitation group was started at 1~2 months after operation
Home control group:Home control group

Sponsors

An Zhen Hospital affiliated to capital medical university
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. patients who were in line with coronary artery bypass grafting (CABG) surgery and planned for CABG surgery; 2. aged 18-70 years old male and female; 3. voluntarily participated in this trial.

Exclusion criteria

Exclusion criteria: 1) there were still unstable angina pectoris after operation; 2) moderate and severe aortic insufficiency; 3) uncontrolled hypertension [pre exercise assessment of systolic pressure > 180mmHg or diastolic pressure > 110mmHg]; 4) with uncontrolled malignant arrhythmia; 5) uncontrolled and symptomatic heart failure; 6) uncontrolled severe infection and operation Postoperative complications; 7) poor healing of incision; 8) combined exercise can lead to deteriorating nervous system, motor system disease or rheumatic disease; 9) patients who are participating in other clinical trials; 10) patients with coronary artery bypass grafting with valve repair, valve replacement, large vascular replacement and other hand surgery; 11) not willing to cooperate with the follow-up.

Design outcomes

Primary

MeasureTime frame
Maximum oxygen uptake;Cardiopulmonary exercise test analysis;Physical fitness;6 minute walk test;

Secondary

MeasureTime frame
Human body composition;Quality of life;Echocardiography;

Countries

China

Contacts

Public ContactQingyu Kong

Anzhen Hospital Affiliated to Capital Medical University

kongqingyu@126.com+86 18911662807

Outcome results

None listed

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