Skip to content

A Randomized Controlled Trial of Electric Fire Needle Therapy for Lower Limb Venous Stasis Dermatitis in Bedridden Patients

A Randomized Controlled Trial of Electric Fire Needle Therapy for Lower Limb Venous Stasis Dermatitis in Bedridden Patients

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2026001434
Enrollment
Unknown
Registered
2026-06-08
Start date
2026-01-01
Completion date
Unknown
Last updated
2026-06-22

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

Conditions

Venous Stasis Dermatitis of the Lower Extremity

Interventions

Electric Fire Needle Unit:Electric Fire Needle
Control Group:Halcinonide Cream

Sponsors

Beijing Aerospace General Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Meets the diagnosis of lower extremity venous stasis dermatitis (varicose eczema); 2. Disease staging follows the CEAP classification system, meeting the criteria for subclass C4a, where C4a is characterized by pigmentation or eczema, presenting as skin pigmentation or eczema, possibly accompanied by itching or skin thickening; 3. No use of antihistamines or other immunosuppressive drugs within the past 6 weeks; 4. Age between 40 and 80 years; 5. Voluntarily participates in the entire study, able to complete medical information forms and sign a written informed consent form.

Exclusion criteria

Exclusion criteria: 1. Patients with any of the following conditions: bleeding disorders, coagulation disorders, immunodeficiency, or history of major bleeding; severe chronic diseases such as cardiovascular, cerebrovascular, liver, or kidney diseases; poorly controlled diabetic patients; acute infectious diseases or fever (body temperature =37.3?); patients with impaired consciousness or mental disorders. 2. Patients with a history of needle syncope or blood syncope, or those allergic to the drugs used in this study. 3. Patients in the pregnancy or lactation period, or those with a tendency to keloid formation. 4. Patients with severe psychological fear or unwillingness to undergo moxibustion therapy. 5. Patients who have participated in other clinical trials within the past 14 days. 6. Patients who have a history of systemic corticosteroid use, specific immunotherapy, or desensitization therapy within the past 3 months prior to enrollment. 7. Other situations deemed unsuitable for participation in clinical research by the investigator.

Design outcomes

Primary

MeasureTime frame
Overall Efficiency;

Secondary

MeasureTime frame
Efficacy Index;Itching VAS score;EASI Scoring;VCSS Score;DLQI Score;Recurrence rate;

Countries

China

Contacts

Public ContactHui Xin

Beijing Aerospace General Hospital

jeshui@126.com17812001692

Outcome results

None listed

Source: ITMCTR (via WHO ICTRP) · Data processed: Jun 29, 2026