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Short-Term Exenatide Therapy in Acute Ischaemic Stroke - A Randomised, Open-Label, Parallel-Group Study

Short-Term Exenatide Therapy in Hyperglycaemia and Acute Ischaemic Stroke - A Randomised, Open-Label, Parallel-Group Study to Determine the Effect of Exenatide on Blood Glucose Levels

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12614001189617
Acronym
GLP-1 and Acute Stroke
Enrollment
9
Registered
2014-11-12
Start date
2015-03-20
Completion date
2017-04-28
Last updated
2020-01-13

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

Conditions

None listed

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

Continuous intravenous administration of 20ug exenatide per 24 hours for up to 72 hours.

Sponsors

Northern Sydney Local Health District
Lead SponsorGovernment body

Study design

Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Treatment
Masking
Open (masking not used)

Eligibility

Sex/Gender
All
Age
18 Years to No maximum
Healthy volunteers
No

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

Outcome results

None listed

Source: ANZCTR · Data processed: Mar 2, 2026