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

NCT ID: NCT06525415

Last Updated: 2024-07-29

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

NOT_YET_RECRUITING

Total Enrollment

30 participants

Study Classification

OBSERVATIONAL

Study Start Date

2024-08-01

Study Completion Date

2024-11-30

Brief Summary

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We investigate the peri-operative foot perfusion through dynamic contrast enhanced MRI in patients with peripheral artery disease

Detailed Description

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Conditions

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Peripheral Arterial Disease Perfusion

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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PAD group

patients of peripheral artery disease who underwent endovascular treatment

DCE MRI

Intervention Type DIAGNOSTIC_TEST

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

Interventions

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DCE MRI

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

Intervention Type DIAGNOSTIC_TEST

Eligibility Criteria

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Inclusion Criteria

* 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.

Exclusion Criteria

* 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;
* Life expectancy\<12 months.
Minimum Eligible Age

18 Years

Maximum Eligible Age

80 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Fudan University

OTHER

Sponsor Role lead

Responsible Party

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Zhijun Bao

Director

Responsibility Role PRINCIPAL_INVESTIGATOR

Other Identifiers

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2024ZW001

Identifier Type: -

Identifier Source: org_study_id

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