Status:

RECRUITING

Comparative Clinical Efficacy Between Multi-layer Bandage Pressure Therapy and Gradient Pressure Elastic Stocking Treatment After Endovenous Radiofrequency Ablation

Lead Sponsor:

Chengdu University of Traditional Chinese Medicine

Conditions:

Vascular Diseases, Peripheral

Venous Insufficiency of Leg

Eligibility:

All Genders

18-80 years

Phase:

NA

Brief Summary

Objective: To assess the clinical efficacy of different compression methods within 48 hours after endovenous radiofrequency ablation (RFA) in terms of great saphenous vein closure rate, postoperative ...

Detailed Description

Postoperative compression of varicose veins can achieve compression hemostasis, early getting out of bed, reducing edema, preventing phlebitis, ensuring closure effect, reducing soreness and pain, and...

Eligibility 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

Key Trial Info

Start Date :

August 1 2023

Trial Type :

INTERVENTIONAL

Allocation :

ESTIMATED

End Date :

August 1 2024

Estimated Enrollment :

210 Patients enrolled

Trial Details

Trial ID

NCT06366763

Start Date

August 1 2023

End Date

August 1 2024

Last Update

April 16 2024

Active Locations (1)

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Hospital of Chengdu University of Traditional Chinese Medicine

Chengdu, Sichuan, China, 610000