None listed
Conditions
Brief summary
As hyperglycaemia in acute ischaemic stroke is associated with increased infarct size and worse functional outcomes, therapies that can maintain normoglycaemia during stroke are of significant clinical importance. GLP-1 analogues, including exenatide, are a potential therapeutic option for the effective regulation of blood glucose levels in acute stroke, without the risk of inducing hypoglycaemia, which can be associated with intensive insulin therapy. GLP-1 therapy is more straightforward to implement and does not require dose adjustment over time, as is necessary for intensive insulin therapy. This may result in less of a burden on treating clinical staff. Furthermore, administration of GLP-1 may have direct beneficial effects on neuronal cell survival and result in neuroprotection, as suggested by animal studies and preliminary clinical data. Thus, the use of a GLP-1 receptor agonist in the management of hyperglycaemia in acute ischaemic stroke (AIS) may confer a benefit in morbidity and mortality for patients long-term.
Interventions
Sponsors
Study design
Eligibility
Inclusion criteria
- Patient presenting with acute ischaemic stroke, as confirmed by routine neurological assessment - Blood glucose level > 10mmol/L on blood glucose testing during the first 72 hours after admission to the Acute Stroke Ward - Age > 18 years
Exclusion criteria
- Type 1 diabetes mellitus - Initial NIHSS > 20 - Life expectancy below 12 months - Pre morbid modified Rankin Score above 3 - Impaired liver function, defined as alanine aminotransferase (ALT) > 3 times the upper limit of normal - Impaired renal function, defined as eGFR < 30 ml/min/1.73m2 - History of pancreatitis - History of pancreatic cancer - History of medullary thyroid cancer or multiple endocrine neoplasia II - Known allergy to exenatide - Suspected or known abuse of alcohol or narcotics - Pregnancy or lactation