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Elastic stockings after varicose vein surgery: useful or nonsense.

Efficacy of routine elastic stockings after varicose vein surgery: a prospective randomised trial.

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON20732
Enrollment
270
Registered
2009-05-22
Start date
2009-04-01
Completion date
Unknown
Last updated
2024-02-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

The standard surgical treatment for varicose veins is stripping of the greater saphenous vein. More recently minimally invasive techniques like endovenous laser therapy of the incompetent greater saphenous vein have gained increasing popularity. Post-operatively after both techniques, patients usually receive compression therapy with elastic stockings. However, no evidence is available to support this routine and frequently the patients experience discomfort from the use of these stockings.

Interventions

Patients will receive elastic stockings (class II) up to the thigh during the day for two weeks. Stockings with a pressure gradient are used for treatment of venous insufficiency. These stockings are

Sponsors

Hulsewé Dr. Karel Chirurg Orbis Medisch Centrum Dr. H. van der Hoffplein 1 Postbus 5500 6130 MB Sittard Nederland k.hulsewe@orbisconcern.nl
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Age between 18 and 65 years; 2. Duplex-proven varicose veins with insufficient saphenofemoral crosse; 3. CEAP-classification: C2-4EpAs,pPr; 4. Informed consent; 5. Suitable for surgical treatment and/or endovenous laser therapy.

Exclusion criteria

Exclusion criteria: 1. Pregnancy; 2. Refusal of informed consent; 3. Deep venous thrombosis in medical history; 4. Previous surgery to vascular structures in lower extremities; 5. Secondary varicose veins; 6. Ulcerative lesions on lower extremities; 7. Contra-indication for use of elastic stockings.

Design outcomes

Primary

MeasureTime frame
The primary endpoint of the study is the pain score. Pain will be measured using a visual analogue scale. In the first week patients will keep score of their pain daily and in the following 5 weeks they will register their pain scores weekly. We will investigate the difference between the group with and the group without elastic stockings in these parameters.

Secondary

MeasureTime frame
1. Presence of complications (deep venous thrombosis, haematoma, thrombophlebitis, wound-infections, oedema); 2. Time before returning to work (or hobby or sports); 3. Analgesics consumption; 4. Leg volume; 5. Functioning- and Varicose vein-scores (RAND-36, AVVQ).

Contacts

Public ContactJ. Elderman

Postbus 5500

j.elderman@orbisconcern.nl

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)