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The feasibility study of multimodal imaging technology in the application of foot perfusion

The feasibility study of multimodal imaging technology in the application of foot perfusion

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600116726
Enrollment
Unknown
Registered
2026-01-14
Start date
2026-02-23
Completion date
Unknown
Last updated
2026-01-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Critical Limb-Threatening Ischemia

Interventions

Group A (Healthy Volunteers):None
Group B (Diabetic Foot Patients):None

Sponsors

The First Affiliated Hospital of Dalian medical University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Group A (Healthy Volunteers) 1.Aged 18–35 years;2.Denies history of vascular diseases, diabetes, foot injury, or foot pain;3.BMI <= 25. Group B (Diabetic Foot Patients) 1.Aged 18–70 years;2.Diagnosed with lower extremity arterial ischemic disease (Rutherford Grade 5–6); 3.Requires endovascular treatment (e.g., balloon angioplasty, stent implantation, etc.); 4.Has signed the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Persons with non-removable magnetic metal implants in the body (such as cardiac pacemakers, certain nerve stimulators, metal internal fixation plates/nails, etc.); 2. Acute lower extremity arterial embolism or thrombosis; 3. Pregnant or lactating women;

Design outcomes

Primary

MeasureTime frame
Image quality (including SNR, contrast, resolution, etc.);

Secondary

MeasureTime frame
Surgical success rate;Changes of task scanning parameters in group A and postoperative scanning parameters in group B;

Countries

China

Contacts

Public ContactDonghua Ji

The First Affiliated Hospital of Dalian medical University

nickji@126.com+86 133 2222 8263

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026