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Study on the Application Value of One-stop Multidimensional Evaluation System of Multimodal Ultrasound in Grading and Prognosis Evaluation of Chronic Venous Insufficiency

Study on the Application Value of One-stop Multidimensional Evaluation System of Multimodal Ultrasound in Grading and Prognosis Evaluation of Chronic Venous Insufficiency

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2200065732
Enrollment
Unknown
Registered
2022-11-14
Start date
2022-11-30
Completion date
Unknown
Last updated
2023-05-15

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

Conditions

chronic venous insufficiency (CVI)

Interventions

Case series:None

Sponsors

Beijing Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients with chronic venous insufficiency of unilateral lower extremity clinically diagnosed and ready for surgery or treatment. Clinical diagnosis of unilateral lower limb chronic venous insufficiency: one side of the lower limb vein is normal (can be accompanied by subclinical reflux, reflux time 1s; 2. Great saphenous vein valve dysfunction, reflux time > 1s; 3. Varicose veins, swelling and pigmentation of lower extremities, with or without venous ulcers of lower extremities (C2-C6); 4. Thrombus in deep venous system of lower extremities (femoral and popliteal veins) (acute stage).

Exclusion criteria

Exclusion criteria: 1. Moderate to severe stenosis and occlusion of either lower limb artery on both sides; 2. Patients with arteriovenous fistula or venous malformation in either lower limb; 3. Patients who have had any previous lower limb artery surgery, such as arterial bypass surgery, arterial balloon dilatation surgery, stent implantation, etc. (including but not limited to the above); 4. Previous lower limb vein treatment or surgery, such as other parts of the bypass through lower limb vein sampling, lower limb venous thrombolysis/thrombolysis (including but not limited to the above); 5. History of lower limb arteriovenous trauma or surgical history involving arteriovenous injury; 6. Allergy to contrast media; 7. Do not agree to participate in the examination and do not sign informed consent.

Design outcomes

Primary

MeasureTime frame
time intensity curve;elastic modulus;shear wave velocity;

Secondary

MeasureTime frame
reflux time;

Countries

China

Contacts

Public ContactLiu Zhiwen

Beijing Hospital

liuzhiwen827@163.com+86 18800161733

Outcome results

None listed

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