Considering compression after varicose vein surgery; a randomised controlled trial.

Recruiting

• Conditions: varicose veins - varicosis; 10057165

• Registration Number: NL-OMON32564
• Lead Sponsor: Heelkunde

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 6 May 2024

Recruitment & Eligibility

• Status: Recruiting
• Sex: Not specified
• Target Recruitment: 100

Inclusion Criteria

- Primary uni- or bilateral insufficiency of the greater saphenous vein

Exclusion Criteria

- CEAP C6
- certain non- compliance for wearing bandaging

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<p>Postoperative edema (leg volume) and pain scores are considered primary<br /><br>endpoints. </p><br>

Secondary Outcome Measures

Name	Time	Method
<p>Postoperative complications and limitation of mobilisation are secundary<br /><br>endpoints.</p><br>