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Ambulatory Varicosity avUlsion Later or Synchronised (AVULS)

Ambulatory Varicosity avUlsion Later or Synchronised (AVULS): a randomised trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN76821539
Enrollment
240
Registered
2011-05-20
Start date
2011-04-01
Completion date
Unknown
Last updated
2016-10-17

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. Simultaneous or delayed avulsion of superficial varicosities in the context of endovenous radiofrequency ablation of refluxing truncal veins 2. Avulsions will be delayed by 6 weeks post initial pro

Sponsors

Imperial College London (UK)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Consecutive patients who present to the department of vascular surgery at Charing Cross Hospital, who are willing to participate in the study 2. They must have clinical venous disease affecting either the long saphenous or short saphenous veins 3. They must be over the age of 18 and able to give consent for the study

Exclusion criteria

Exclusion criteria: 1. Patients under the age of 18 years 2. Those that are unable to consent 3. Patients with deep venous disease 4. Those unfit for intervention

Design outcomes

Primary

MeasureTime frame
Disease specific quality of life at 6 months using the Aberdeen Varicose Vein Questionnaire (AVVQ)

Secondary

MeasureTime frame
1. The need for further procedures over the 6 month period 2. Generic quality of life assessed using the EQ-5D 3. Cost effectiveness of the treatment strategies 4. Anatomical success assessed with colour duplex at 6 months 5. Level of depression assessed using Center for Epidemiologic Studies Depression Scale (CES-D) 6. Return to work and normal activities 7. Clinical disease severity assessed using the Venous Clinical Severity Score (VCSS)

Countries

United Kingdom

Outcome results

None listed

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