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NCT06366763

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

Recruiting now NA Last updated 16 April 2024
What this trial tests

NA trial testing Questionnaires in Vascular Diseases, Peripheral in 210 participants. Currently enrolling.

Timeline
1 August 2023
Primary endpoint
1 August 2024
1 August 2024

Quick facts

Lead sponsorChengdu University of Traditional Chinese Medicine
PhaseNA
StatusRecruiting now
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment210
Start date1 August 2023
Primary completion1 August 2024
Estimated completion1 August 2024
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

Chengdu University of Traditional Chinese Medicine

Who can join

Adults 18 to 80, any sex, with Vascular Diseases, Peripheral or Venous Insufficiency of Leg. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

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 complications, quality of life, time to return to normal work, and patient satisfaction.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of Questionnaires

Trials testing the same drug.

Other Chengdu University of Traditional Chinese Medicine trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06366763.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing