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The Glucose Insulin in Stroke Trial (GIST)

The Glucose Insulin in Stroke Trial (GIST)

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN31118803
Enrollment
2500
Registered
2004-01-23
Start date
2002-09-01
Completion date
Unknown
Last updated
2022-09-12

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

Conditions

Cardiovascular diseases: Cerebrovascular disease Circulatory System Stroke

Interventions

1. Treatment with intravenous 10% glucose solution, 20 mmol KCL and Actrapid insulin (initial insulin 16 units/500ml) at 100 ml per hour. 2. Control treatment with intravenous N saline

Sponsors

NHS R&D Regional Programme Register - Department of Health (UK)
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: All acute stroke patients (less than 24 hours onset) with cerebral infarction (CI) or primary intracerebral haemorrhage (PICH) and admission plasma glucose greater than 6.1 and less than 17 mMol/l.

Exclusion criteria

Exclusion criteria: 1. Subarachnoid haemorrhage 2. Renal failure (urea 320 mMol/l or creatinine 3200 mMol/l) 3. Anaemia (Hb less than 9.0 g/dl) 4. Coma 5. Isolated posterior circulation syndromes with no physical disability 6. Pure language disorders 7. Established history of insulin dependent diabetes mellitus 8. Previous disabling stroke (Modified Rankin score 3) 9. Established diagnosis of dementia or abbreviated mental test score less than 7/10 10. Symptomatic cardiac failure - New York Heart Association (NYHA) Grade 3 or 4

Design outcomes

Primary

MeasureTime frame
All-cause mortality at 12 weeks.

Secondary

MeasureTime frame
Proportion of patients with a poor outcome (modified Rankin score 4 - 6) at 12 weeks between treatment groups.

Countries

England, United Kingdom

Outcome results

None listed

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