Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-25 @ 12:31 AM
Ignite Modification Date:
2025-12-25 @ 12:31 AM
NCT ID:
NCT07009067
Eligibility Criteria:
Inclusion Criteria:
* Patients with a previous diagnosis of type B aortic dissection or intramural hematoma or penetrating ulcer, who underwent endovascular aortic repair (EVAR) or EVAR + supra-aortic shunt surgery for more than 1 month, and no related complications (such as endoleak, stent thrombosis, dissection progression, etc.) were found in the postoperative aortic CTA;
* Able to independently carry out basic daily life activities, participants must be able to complete the baseline assessment and start the designated treatment;
* Patients voluntarily participate in this study, sign the written informed consent, and are willing to cooperate with the follow-up;
Exclusion Criteria:
* Acute myocardial infarction occurred 1 month ago;
* Combined with severe aortic stenosis or regurgitation;
* Combined with ascending aortic aneurysm or dissection;
* Acute heart failure occurred 2 weeks ago;
* Combined with severe hypertrophic obstructive cardiomyopathy;
* Chronic renal failure stage 5, which is defined as glomerular filtration rate \<15ml/(min·1.73m2) or dialysis;
* During the screening examination, the patient's alanine aminotransferase or aspartate aminotransferase is greater than or equal to 5 times the upper limit of the normal value specified by our center;
* Patients with any medical history that may affect compliance with the program;
* Patients with severe language, mental or physical disabilities who are unable to participate in the program;
* Pregnant or lactating women, or those with fertility who are unwilling/unable to take effective contraceptive measures;
* Patients participating in other interventional clinical trials;
* Patients with long-term high-intensity exercise habits;
* Patients who are judged by the researchers to be unsuitable for participation in this study;
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Maximum Age:
75 Years
Study:
NCT07009067
Study Brief:
Protocol Section:
NCT07009067