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Surgical glue for the treatment of damaged veins in patients with venous leg ulcers

Pilot study of cyanoacrylate occlusion of the lower limb veins in patients with venous leg ulcers

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN15014758
Enrollment
55
Registered
2018-02-20
Start date
2017-11-06
Completion date
Unknown
Last updated
2019-04-29

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

Conditions

Venous leg ulcer Injury, Occupational Diseases, Poisoning Venous leg ulcer

Interventions

Cyanoacrylate (surgical glue) occlusion plus compression bandaging, wound care and specialist leg ulcer clinician review versus compression bandaging, wound care and specialist leg ulcer clinician rev

Sponsors

University Hospital of South Manchester
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Venous ulcer of the lower limb at least 2cm2 (CEAP classification C6) 2. Ulceration present for >6 weeks and 0.5 seconds duration, confirmed by venous duplex imaging 4. Aged =18 years 5. Willing and able to provide informed consent 6. Ipsilateral ankle-brachial pressure index =0.8 at the time of randomisation

Exclusion criteria

Exclusion criteria: 1. Non-venous cause of ulceration: peripheral arterial disease (ABPI < 0.8), vasculitis, neuropathy, recent lower limb trauma, chronic dermatitis, pyoderma gangrenosum, malignancy, chronic osteomyelitis or any other lower limb pathology that may be contributing to the ulceration, in the opinion of the investigator. 2. Inability to tolerate or comply with lower limb compression therapy 3. Inability to receive prompt endovenous treatment 4. Unwilling or unable to provide informed consent 5. Current enrolment in another study pertaining to venous ulceration 6. Primary or secondary immunosuppression 7. Previous treatment of the target vein or other venous surgery that may compromise the study, in the opinion of the research team 8. Patient has pre-planned surgical intervention or endovascular procedure scheduled up to 30 days after the index procedure 9. Currently pregnant 10. Duplex evidence of deep venous incompetence or occlusion 11. Clinical evidence of post-thrombotic syndrome 12. Incompetent vein considered too tortuous to allow VenaSealTM treatment 13. Inability to tolerate VenaSealTM treatment

Design outcomes

Primary

MeasureTime frame
1. Rate of healing in leg ulcer surface area is measured using tracings of the ulcer area every seven days (+/- 2 days) until the ulcer has healed, in the opinion of the reviewing clinician 2. Time to healing is measured by recording the number of days between the randomisation date and the day on which the clinicians see that the wound has healed

Secondary

MeasureTime frame
1. Quality of life, self-assessment of health, and severity of symptoms is measured using EQ-5D and VEINES-QoL scores 6,7 at baseline, three, six and 12 months 2. Lower limb venous disease is measured using the Venous Clinical Severity Score, at baseline, three, six and 12 months 3. Rate of venous recanalization measured using duplex ultrasound at baseline, three, six and 12 months 4. Patient satisfaction is measured using Likert scale measures in a written questionnaire at baseline, three, six and 12 months 5. Adverse events are measured using reports at 12 months 6. Health economic analysis is measured using the cost and frequency of visits to wound care and outpatient clinic, district nurse visit costs, inpatient treatment costs and costs of complications of the treatment or of non-healing ulcers at baseline, three, six and 12 months

Countries

United Kingdom

Contacts

Public ContactDavid Riding
david.riding@manchester.ac.uk+44 161 292 5842

Outcome results

None listed

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