Aspirin for Venous Ulcers: Randomised Trial (AVURT)

Phase 2TerminatedNCT02333123

St George's, University of London26 enrolled

Overview

This efficacy study evaluates the safety and effectiveness of aspirin for venous leg ulcer healing. The study also examines whether patients can be recruited to a larger study. Patients with chronic venous leg ulceration presenting and undergoing care in leg ulcer community clinics or hospital out-patient clinics, or registered with a clinic but are receiving care at home will be recruited. All patients will receive standard compression bandaging. Half of the participants will be randomised to receive aspirin, while the other half will receive a placebo.

The mainstay of treatment of leg ulcers is graded compression therapy to squeeze the fluid out of the leg and venous system. This has been shown to be effective in many clinical trials. However, despite this treatment patients take many months to heal (with median healing times of approximately 12 weeks in previous trials) and for some patients compression therapy does not result in resolution of their leg ulcers. The use of compression (as well as dressings largely to manage the wound exudate) can be expensive as nurse time is required to change bandages which can be required weekly or more frequently. Furthermore, for many patients the compression therapy is uncomfortable (sometimes painful) and inconvenient for everyday life (compression is bulky and dressings have to be changed several times weekly). If other treatments were able to reduce the time to healing then this would be a significant breakthrough. Results from two earlier small trials suggest aspirin may be of benefit. However this trials were poorly designed and reported. The present study will evaluate whether the addition of 300mg of daily aspirin to standard evidence based therapies reduces the time to healing of chronic venous leg ulceration using a more rigorous design. The study will also establish the feasibility of satisfactory participant recruitment for a bigger trial, and whether participants are compliant with their aspirin therapy. The safety of aspirin in this patient population will also be monitored.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

TREATMENT

Masking

QUADRUPLE

Enrollment

Conditions

Venous Leg Ulcer

Interventions

AspirinDRUG

Each 300mg aspirin capsule will contain over-encapsulated 4 x Aspirin 75mg tablets.

Placebo (for Aspirin)DRUG

Each placebo capsule will contain a lactose and magnesium stearate blend, and will appear identical in weight, colour and size to the matched aspirin capsules.

Eligibility

Sex: ALLMin age: 18 Years

Medical Language ↔ Plain English

Inclusion Criteria: * Those with at least one chronic venous leg ulcer - where chronic venous leg ulceration is defined as any break in the skin which has either: a) been present for more than six weeks, or b) occurred in a person with a history of venous leg ulceration. Ulcers will be considered purely venous if clinically no other etiology was suspected. For this the ulcer must be venous in appearance (i.e. moist, shallow, of an irregular shape) and lie wholly or partially within the gaiter region of the leg. If the patient has more than one ulcer we will choose the largest ulcer as the 'index' lesion for purposes of the analysis. * Ulcer area \> 1 square cm * Participants must have had an ankle brachial pressure index (ABPI) ≥ 0.8 taken within the previous three months. When the ABPI is incompressible other forms of assessment including peripheral pulse examination / toe pressure / duplex ultrasound in combination with clinical judgement to be used to exclude PAD * Aged ≥ 18 years (no upper age limit) * Able and willing to provide informed consent * Ulcer duration \> 6 weeks or prior history of venous ulceration. Exclusion Criteria: * Unable to provide consent * Unwilling to provide consent * Foot (below the ankle) ulcer * A leg ulcer of non-venous aetiology (i.e. arterial) * Ankle-brachial pressure index (ABPI) \<0.8 * Current regular use of aspirin (as may be randomised to placebo) * Previous intolerance of aspirin / contraindication to aspirin (decision made according to the prescribers' clinical judgement) * Prohibited medication: Probenecid * Known lactose intolerance (as placebo contains lactose) * Pregnant/lactating women * Currently participating in another study evaluating leg ulcer therapies. * Another reason that excluded them from participating within this trial (decision made according to the nurses' or prescribers' clinical judgment )\* * Previously been recruited in to this trial.

Locations (5)

Hull & East Yorkshire Hospital NHS Trust

Cottingham, Castle Hill Hosp, United Kingdom

St George's University Hospitals NHS Foundation Trust

Tooting, London, United Kingdom

Harrogate & district NHS Trust

Harrogate, N.Yorkshire, United Kingdom

Brighton General Hosp

Brighton, Sussex, United Kingdom

Outcomes

Primary Outcomes

Time to healing of the reference ulcer (the largest eligible ulcer)

Time frame: 25 weeks

Secondary Outcomes

Ulcer size (area) measured in square cm

Time frame: 25 weeks

Recurrence of reference ulcer

Proportion of participants with a recurrence of reference ulcer. Time to recurrence.

Time frame: 25 weeks

Ulcer related pain using the VAS Score

Time frame: 5 weeks

Treatment concordance: number of participants completing the course of treatment

Proportion of participants completing the course of treatment up to healing or planned trial exit. The number of capsules taken. Nurse's assessment of participant's compliance with recommended compression therapy.

Time frame: 24 weeks

Resource use

Number and duration of all leg ulcer-related appointments with health professionals (including wound related in-patient stays ). Number of and types of dressings used.

Time frame: 27 weeks

Number of adverse events

Number of participants with at least one event. Total number of events.

Time frame: 27 weeks

Data from ClinicalTrials.gov

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