ClinicalTrials.Veeva

Menu

Compression Treatment of Superficial Vein Thrombosis

Medical University of Vienna logo

Medical University of Vienna

Status

Completed

Conditions

Erythema
Quality of Life
Pain
Thrombus Length

Treatments

Other: no compression
Device: compression

Study type

Interventional

Funder types

Other

Identifiers

NCT01976637
EKNr 772/2009

Details and patient eligibility

About

Leg compression is considered the basic treatment for superficial vein thrombosis (SVT). However, its use is more or less based on subjective experience while scientific evidence for its efficacy is lacking. There is one uncontrolled trial reporting improvement of clinical symptoms when patients with SVT were treated with fixed compression bandages.

This study evaluates the efficacy of compression stockings (23-32 mmHg) in the treatment SVT of the legs. The investigators hypothesis is that compression treatment is superior to no compression in alleviating disease related clinical symptoms.

Enrollment

80 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • patients with superficial vein thrombosis of the leg,
  • thrombus extent of at least 5 cm confirmed by duplex sonography,
  • clinical signs of inflammation (pain, erythema)

Exclusion criteria

  • superficial thrombus distance to the saphenofemoral or saphenopopliteal junction of less than 2cm,
  • concomitant deep vein thrombosis,
  • thrombophilia,
  • active malignoma,
  • immobility,
  • peripheral arterial occlusive disease,
  • superficial vein thrombosis after sclerotherapy
  • incision and clot expression
  • excessive leg configuration not covered by ready made compression stockings

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

80 participants in 2 patient groups

no compression
Experimental group
Description:
no compression stockings worn during a 3 weeks period
Treatment:
Other: no compression
compression stockings
Active Comparator group
Description:
compression stockings class II (23-32 mm Hg) worn during the day for up to 3 weeks
Treatment:
Device: compression

Trial contacts and locations

0

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems