MedTrace Logo

Compression And Functional Ability After Endovenous Varicose Vein Treatment

NCT03613376 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 109

Last updated 2021-01-20

No results posted yet for this study

Summary

Study's aim is to study possible differences in post-operative rehabilitation, functional ability and visual disturbances after endovascular varicose intervention (RF-catheter and foam sclerotherapy) in two study groups, where patients will be randomised to either no compression group (Group I) or compression group (Group II)

Conditions

  • Varicose Veins of Lower Limb
  • Varicose Veins

Interventions

OTHER

Class II compression stockings

Patients in this group will use class II compression stocking continuously until next evening and then next 4 days during daytime

Sponsors & Collaborators

  • Oulu University Hospital

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
80 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-05-21
Primary Completion
2020-12-21
Completion
2021-01-01

Countries

  • Finland

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03613376 on ClinicalTrials.gov