Comparing two compression methods after varicose vein treatment
Comparative Clinical Efficacy Between Multi-layer Bandage Pressure Therapy and Compression Stockings Treatment After Endovenous Radiofrequency Ablation
This study is testing whether using multi-layer bandages or elastic stockings after varicose vein treatment helps patients feel better and recover more effectively.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 210 (estimated) |
| Ages | 18 Years to 80 Years |
| Sex | All |
| Sponsor | Chengdu University of Traditional Chinese Medicine Academic / other |
| Locations | 1 site (Chengdu, Sichuan) |
| Trial ID | NCT06366763 on ClinicalTrials.gov |
What this trial studies
This study evaluates the effectiveness of multi-layer bandage pressure therapy versus gradient pressure elastic stockings in patients who have undergone endovenous radiofrequency ablation for varicose veins. It aims to assess outcomes such as vein closure rates, postoperative complications, quality of life, and patient satisfaction within 48 hours post-procedure. The study addresses the discomfort associated with traditional compression methods and seeks to provide evidence for optimal postoperative care. Participants will be monitored for a month following the intervention to determine the best approach to compression therapy.
Who should consider this trial
Good fit: Ideal candidates are adults aged 18 to 80 with symptomatic varicose veins eligible for radiofrequency ablation.
Not a fit: Patients with severe deep vein valve insufficiency or acute deep vein thrombosis will not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved postoperative care and comfort for patients undergoing varicose vein treatments.
How similar studies have performed: While there is ongoing debate regarding postoperative compression methods, this study aims to fill a gap in evidence, suggesting a novel approach to a common postoperative issue.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Age \>18 years and \<80 years, and able to understand the requirements of the study and provide informed consent and accept the exams and follow-up. * C2 - C5 varicose veins / CVI Symptomatic primary GSV, SSV, or AASV incompetence, with reflux \>0.5 seconds on color duplex, eligible for patients undergoing radiofrequency ablation. * Color replica ultrasound or venography of the lower extremity veins shows saphenous varicose veins without evidence of deep venous stenosis, filling defects, or ultrasound abnormalities. * No contraindications to the wearing of compression stockings (e.g., arterial insufficiency, skin allergies) Exclusion Criteria: * Severe deep vein valve insufficiency or acute deep vein thrombosis of the lower extremities * Previous history of high ligation and dissection of the saphenous vein, recurrence of collateral branches of the deep vein * Superficial vein thrombosis is present at the treatment site, with local redness, swelling, warmth, pain, and significant signs of inflammation
Where this trial is running
Chengdu, Sichuan
- Hospital of Chengdu University of Traditional Chinese Medicine — Chengdu, Sichuan, China (Recruiting)
Study contacts
- Study coordinator: Chunshui He, Doctor
- Email: chunshuihe@msn.com
- Phone: 18981885601
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.