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Venous Pressure Monitoring in Patients Undergoing Foam Sclerotherapy

Continuous Ambulatory Venous Pressure Monitoring and the Results of Foam Sclerotherapy in the Lower Limb

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ISRCTN
Registry ID
ISRCTN00165319
Enrollment
36
Registered
2010-09-29
Start date
2010-10-15
Completion date
Unknown
Last updated
2017-12-18

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

Conditions

Varicose veins Circulatory System Varicose veins of lower extremities

Interventions

1. Recruitment: Patients will be recruited from outpatient clinics held at the Queen Elizabeth Hospital and Freeman Hospital. Three patient groups, determined by the anatomical site of venous reflux w

Sponsors

Gateshead Health NHS Foundation Trust (UK)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Patients with long or short saphenous venous reflux 2. Patients with varicose veins belonging to any of the clinical classes of Clinical, Etiologic, Anatomic and Pathophysiologic (CEAP) classification C2, C3, C4, C5 and C6 3. Patients with a full range of movement of the joints in both their lower limbs 4. Patients who are freely mobile with no mechanical aid assisting their movement 5. Aged 18 - 75

Exclusion criteria

Exclusion criteria: 1. Patients belonging to CEAP Ec, Po and Po & R or with past history of Deep Vein Thrombosis (DVT) or pulmonary embolism 2. A history suggestive of deep venous obstruction 3. Peripheral arterial disease 4. Anticoagulation therapy 5. Serious systemic diseases such as angina, myocardial infarction, asthma, COAD, CCF, hepatic failure and renal failure 6. Pregnancy 7. Any patent with heparin allergy 8. Patients unable to give consent

Design outcomes

Primary

MeasureTime frame
To quantify and assess the venous pressure-lowering effect of Foam Sclerotherapy in patients with lower limb superficial venous reflux and to compare the venous pressures with patients' activity profiles. These measurements will be performed using a Continuous Ambulatory Venous Pressure Monitoring device and a NUMACT system

Secondary

MeasureTime frame
To assess changes in quality of life associated with foam sclerotherapy treatments using the Aberdeen Varicose Vein Questionnaire.

Countries

United Kingdom

Outcome results

None listed

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