Skip to content

Prospective, controlled trial on safety and efficacy of compression stockings for patients with CVI and pAVK (Angioflow2)

Prospective, controlled trial on safety and efficacy of compression stockings for patients with CVI and pAVK (Angioflow2) - Angioflow 2

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00013978
Enrollment
55
Registered
2018-02-09
Start date
2018-02-05
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

I73.9 I87.2 I70.2

Interventions

Group 1: Wearing the compression stocking on the leg with the lowest ankle brachial index (ABI) and concomitant chronic venous insufficiency (CEAP criteria C3-C5)

Sponsors

St. Josef und St. Elisabeth Hospital gGmbHKlinik für Dermatologie, Venerologie und Allergologie
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: - Age > 18 years old - Chronic venous insufficiency of any genesis (varicose disease, PTS, arthrogenic congestion syndrome, dependency syndrome in obesity) in stages C3 to C5. - ability to put on compression stockings or willingness to have them worn by third parties - Written consent form - Willingness to wear compression stockings of at least 8 hours per day during the study period - Peripheral arterial occlusive disease with an ankle arm index 0.5 and an absolute ankle arterial pressure >60mmHg

Exclusion criteria

Exclusion criteria: - Pregnant or nursing patient - Patient participating in another treatment study Patients with severe general illness for whom there is a risk of withdrawal before the end of the study. - Patient with progressive malignant disease, associated with radiation therapy, Chemotherapy or hormone therapy treated. - allergy to components of the compression stocking - Absolute contraindication for an compression therapy: decompensated Heart failure, septic phlebitis, Phlegmasia coerulea dolens. - Acute deep or superficial leg vein thrombosis - disability or reluctance, put on compression stockings or to be worn florides Ulcus cruris, C6

Design outcomes

Primary

MeasureTime frame
Complaint score measured by the Varicose Vein Symptom Questionnaire Acral pressure measured by means of acral oscillography

Secondary

MeasureTime frame
- Leg volume, measured by Bodytronic 600®. - Semiquantitative assessment of leg edema by ultrasound - Visual analogue scale for pain (0=no pain, 10=strongest pain) - Visual analogue scale for ease of use (pull stocking over the foot, Suspender stocking overall, stocking take off) - Wearing comfort of the compression stocking, measured as patient satisfaction on a visual analogue scale. - Anamnestic painless walking distance

Countries

Germany

Contacts

Public ContactStefanie Reich-Schupke

Venenzentrum der Dermatologischen und Gefäßchirurgischen KlinikenKliniken der Ruhr-Universität Bochum im St. Maria Hilf Krankenhaus

s.reich-schupke@klinikum-bochum.de+49 234 8792 270/274

Outcome results

None listed

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