Effect of Enhanced External Counterpulsation (NCT06877390) | Clinical Trial Compass
CompletedNot Applicable
Effect of Enhanced External Counterpulsation
China60 participantsStarted 2023-11-01
Plain-language summary
This study evaluated the efficacy and safety of enhanced extracorporeal counterpulsation for cardiac rehabilitation in patients after DCB for acute myocardial infarction.
Who can participate
Age range18 Years – 75 Years
SexALL
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Inclusion Criteria:
* patients with AMI diagnosed based on the universal definition of myocardial infarction criteria
* a single vessel infarcted, and Syntax score ≤22
* patients treated using DCB
* patients without EECP contraindications
* patients aged 18-75 years
* patients who had signed informed consent and were able to cooperate in completing the study
Exclusion Criteria:
* patients with lower limb deep venous thrombosis and active thrombophlebitis
* patients with moderate to severe valvular heart disease, especially those with aortic insufficiency and/or stenosis
* patients with moderate to severe pulmonary arterial hypertension (mean pulmonary arterial pressure \>50 mmHg)
* patients with aortic, cerebral or dissecting aneurysms
* patients with uncontrolled hypertension (\>180/110 mmHg)
* patients with decompensated heart failure (cardiac function of grade IV)
* patients with arrhythmia that might interfere with the electrocardiographic gating function of the EECP device
* patients with haemorrhagic diseases or obvious bleeding tendencies
* patients with infected lesions in their limbs that may affect EECP
* pregnant women
* patients with ventricular aneurysm and mural thrombus detected through echocardiography
What they're measuring
1
Comparison of baseline data
Timeframe: followed up for 6 months
2
Comparison of baseline data
Timeframe: followed up for 6 months
3
Comparison of baseline data
Timeframe: followed up for 6 months
4
Comparison of baseline data
Timeframe: followed up for 6 months
5
Comparison of baseline data
Timeframe: followed up for 6 months
6
Comparison of baseline data
Timeframe: followed up for 6 months
7
Comparison of baseline data
Timeframe: followed up for 6 months
8
Comparison of baseline data
Timeframe: followed up for 6 months
9
Comparison of cardiac function
Trial details
NCT IDNCT06877390
SponsorChongming Hospital Affiliated to Shanghai University of Health & Medicine Sciences