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Clinical application of new elastic socks in patients with venous insufficiency of lower extremity

Clinical application of new elastic socks in patients with venous insufficiency of lower extremity

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100042894
Enrollment
Unknown
Registered
2021-01-31
Start date
2021-02-01
Completion date
Unknown
Last updated
2021-05-17

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

Conditions

Chronic venous insufficiency

Interventions

experimental group:New elastic socks
Control group:Ordinary elastic socks
Control group:Elastic socks with weak pressure

Sponsors

Beijing Chaoyang Hospital, Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Aged 18-75 years, signed informed consent; 2. Diagnosis of chronic venous insufficiency of lower extremity; 3. Ankle brachial index (ABI) > 0.85; 4. Inclusion criteria of lesions: (1) color Doppler ultrasound showed femoral vein valve regurgitation; (2) femoral vein valve closure time > 0.5s; (3) diameter of perforating vein > 2.5mm.

Exclusion criteria

Exclusion criteria: 1. Use diuretics, dihydroergotamine or other drugs with intravenous activity at the same time; 2. Pregnant or lactating women; 3. There are factors that affect ulcer wound healing: hormone use, diabetic patients; 4. Cardiac or renal edema 5. Those who could not follow the requirements of the study protocol (such as uncooperative attitude, unable to follow-up and / or other situations that the researchers thought that the study could not be completed), resulting in the failure to implement nursing measures; those who dropped out due to various reasons; 6. Those with lower limb infection could not be treated with medical elastic socks; 7. Those in critical condition could not be treated with physical therapy. 8. To participate in other clinical drug or device research within 6 months before the start of the study. 9. To explore the reasons why other researchers think it is not suitable to participate in this study.

Design outcomes

Primary

MeasureTime frame
Lower limb data measurement;

Secondary

MeasureTime frame
Lower extremity vascular ultrasound;Ankle brachial index;

Countries

China

Contacts

Public ContactLi Chunmin

Beijing Chaoyang Hospital, Capital Medical University

lcmbs@126.com+86 15210091286

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 5, 2026