About this trial
We investigate the peri-operative foot perfusion through dynamic contrast enhanced MRI in patients with peripheral artery disease
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
18 to 80 years old;
PAD patients with Fontaine grade II-IV or Rutherford grade 2-6 and underwent a successful revascularization;
Patients completed both pre- and post-operative MRI workups;
Patients signed the informed consent form and be able to complete the clinical follow-up for 1 months.
Disqualifiers
Patients has participated in other clinical studies;
Patients with Heart failure (NYHA III/IV)/right to left shunt heart disease/ severe aortic and mitral insufficiency/acute coronary syndrome/malignant arrhythmia/severe pulmonary hypertension (pulmonary artery pressure at least 90 mmHg)/moderate to severe renal insufficiency (creatinine clearance rate<60 ml/min)
Any allergic constitution;
Pregnancy and childbirth;
Trial population
patients with peripheral artery disease, who had a successful endovascular treatment and completed both pre- and post-operative MRI workups
Trial design
Cohort
Prospective
Treatments tested in this trial
DCE MRI
Diagnostic testthe recruited patients should complete pre- and post-operative DCE MRI workshops
Treatment groups
Trial outcomes
Primary outcomes
preoperative perfusion parameters
preoperative perfusion parameters by dynamic contrast-enhanced (DCE) magnetic resonance imaging (MRI)
Secondary outcomes
ankle brachial index
clinical success
survival
Locations
Sponsors and contacts
Click on the lead sponsor to view all of their trials.
This trial is not recruiting at the moment. You can still explore other options: