Influence of compression stockings on skin moisture and quality of life in patients with chronic venous insufficiency

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

DRKS

Registry ID

DRKS00022526

Enrollment

Registered

2020-11-13

Start date

2020-11-03

Completion date

Unknown

Last updated

2025-04-07

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

Conditions

I87.2

Interventions

Group 1: vrum group - compression stocking with integrated palmitoylethanolamide Group 2: placebo group - compression stocking without special ingredients

Eligibility

Sex/Gender

All

Age

18 Years to 85 Years

Inclusion criteria

Inclusion criteria: a) patients with chronic venous insufficence b) age betwenn 18 an 85 c) willingness to wear compression stockings d)existence of a written patient agreement f) sufficient german speaking skills

Exclusion criteria

Exclusion criteria: a) age under 18 years b) edema of the leg that are not caused by a CVI c) deep vein thrombosis of the leg d) peripheric arterial occlusion e) diabetes with neuropathy or a periperial arterial disturbed blood flow f) immobility g) ulcus cruris venosum h) pregnancy i) customization

Design outcomes

Primary

Measure	Time frame
skin moisture is measured by corneometry on day 0, after two weeks and after four weeks	—

Secondary

Measure	Time frame
qulity of life, compliance, pain, pruritus, heavy legs	—

Countries

Germany

Contacts

Public ContactIsabell Rüdiger

Bauerfeind AG

isabell.ruediger@bauerfeind.com015228824611

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026