Leg Ischaemia Management Collaboration

Recruiting Observational Study
Peripheral Arterial Disease Critical Limb Ischemia Frailty Cognitive Impairment Coronary Artery Disease
No Placebo Group Every participant receives an active treatment — no one gets a placebo. No Study Drug Researchers observe your health over time — no experimental treatment is given.
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At a Glance
Age
18 – 110
Sex
Any
Study type
Observational
Participants needed
420 (estimated)
Sponsor
University of Leicester · Other
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About This Trial
Single-centre prospective cohort study of patients presenting with severe limb ischaemia (SLI). The primary outcome measure will be 12 month major amputation rate. A historical cohort of patients identified retrospectively will be the comparitor group used to assess the impact of a newly-established rapid-access limb salvage clinic. Primary aim: \- Determine the proportion of patients with SLI u…
Trial Locations
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Eligibility Criteria
PRIMARY COHORT Inclusion Criteria: * All patients presenting to the Leicester Vascular Institute with SLI Exclusion Criteria: * SLI not caused by PAOD * Patients undergoing intervention during their index presentation prior to recruitment * Patients lacking capacity to consent with no accompanyi…
Contacts

Rob D Sayers, MD

+44 (0)116 252 3141

rs152@le.ac.uk

CONTACT

Tanya J Payne, BSc

+44 (0)116 258 3867

tjp28@le.ac.uk

CONTACT