Foot Perfusion by Dynamic Contrast Enhanced MRI in Patients With Peripheral Artery Disease

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-80
SponsorFudan University

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 volunteers

Qualifiers

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

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

  • DCE MRI

    Diagnostic test

    the recruited patients should complete pre- and post-operative DCE MRI workshops

Treatment groups

30 Participants
are divided into 1 treatment group
Group A: PAD group1 intervention

Trial outcomes

Primary outcomes

1

preoperative perfusion parameters

preoperative perfusion parameters by dynamic contrast-enhanced (DCE) magnetic resonance imaging (MRI)

Time frame
Between Aug.1 2024 and OCT.31 2024

Secondary outcomes

1

ankle brachial index

Time frame
Between Aug.1 2024 and OCT.31 2024
2

clinical success

Time frame
Between Aug.1 2024 and NOV.30 2024
3

survival

Time frame
Between Aug.1 2024 and NOV.30 2024

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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