Stroke Hyperglycemia Insulin Network Effort (SHINE) Trial
Status: | Active, not recruiting |
---|---|
Conditions: | Neurology, Diabetes |
Therapuetic Areas: | Endocrinology, Neurology |
Healthy: | No |
Age Range: | 18 - Any |
Updated: | 9/2/2018 |
Start Date: | April 2012 |
End Date: | December 2018 |
The Stroke Hyperglycemia Insulin Network Effort (SHINE) Trial is a multicenter, randomized,
controlled clinical trial of 1400 patients that will include approximately 60 enrolling
sites. The study hypotheses are that treatment of hyperglycemic acute ischemic stroke
patients with targeted glucose concentration (80mg/dL - 130 mg/dL) will be safe and result in
improved 3 month outcome after stroke.
Eligible subjects must be randomized within 12 hours of stroke symptom onset and either have
type 2 diabetes and glucose concentrations of over 110 mg/dL or no history of diabetes and
glucose concentrations of 150 mg/dL or higher on initial evaluation. The enrolling sites will
include the Neurological Emergencies Treatment Trials (NETT) sites as well as non NETT sites
from all over the United States. The study will evaluate the safety and efficacy of targeted
glucose control (treatment group - IV insulin with target 80-130 mg/dl) verses control
therapy of sub q insulin plus basal insulin with target glucose less than 180 mg/ dL. The
primary outcome will be functional outcome at 3 months as measured by the modified Rankin
Scale (mRS) Score. The primary safety outcome will be severe hypoglycemia defined as <40
mg/dL. Enrollment will occur over 5-7 years.
controlled clinical trial of 1400 patients that will include approximately 60 enrolling
sites. The study hypotheses are that treatment of hyperglycemic acute ischemic stroke
patients with targeted glucose concentration (80mg/dL - 130 mg/dL) will be safe and result in
improved 3 month outcome after stroke.
Eligible subjects must be randomized within 12 hours of stroke symptom onset and either have
type 2 diabetes and glucose concentrations of over 110 mg/dL or no history of diabetes and
glucose concentrations of 150 mg/dL or higher on initial evaluation. The enrolling sites will
include the Neurological Emergencies Treatment Trials (NETT) sites as well as non NETT sites
from all over the United States. The study will evaluate the safety and efficacy of targeted
glucose control (treatment group - IV insulin with target 80-130 mg/dl) verses control
therapy of sub q insulin plus basal insulin with target glucose less than 180 mg/ dL. The
primary outcome will be functional outcome at 3 months as measured by the modified Rankin
Scale (mRS) Score. The primary safety outcome will be severe hypoglycemia defined as <40
mg/dL. Enrollment will occur over 5-7 years.
Inclusion Criteria:
1. Age 18 years or older
2. Clinical diagnosis of ischemic stroke defined as acute neurological deficit occurring
in one or more cerebral vascular territories. Neuroimaging must be done to exclude
intracranial hemorrhage (ICH).
3. Randomization must be within 12 hours after stroke symptom onset and treatment is
recommended, but not required, to begin within 3 hours after hospital arrival. If time
of symptom onset is unclear or patient is awakening with stroke symptoms, the time of
onset will be the time the patient was last known to be normal.
4. Known history of type 2 diabetes mellitus and glucose >110 mg/dL OR admission blood
glucose ≥150 mg/dL in those w/o known diabetes mellitus
5. Baseline NIHSS score of 3-22
6. Pre-stroke modified Rankin Scale score = 0 for patients with an NIHSS score of 3-7.
Pre-stroke modified Rankin Scale score = 0 or 1 for patients with an NIHSS score of
8-22.
7. Able to provide a valid informed consent to be in the study (self or their authorized
legally accepted representative). The approved consent form must be signed and dated
in accordance with federal and institutional guidelines.
Exclusion Criteria:
1. Known history of type 1 diabetes mellitus
2. Substantial pre-existing neurological or psychiatric illness that would confound the
neurological assessment or other outcome assessment
3. Having received experimental therapy for the enrollment stroke. IV tPA (up to 4.5 hrs)
or IA tPA are allowed as are IA therapies including use of FDA cleared devices. Non
FDA cleared devices are considered experimental and are excluded.
4. Pregnant or breast-feeding at the time of study entry
5. Other serious conditions that make the patient unlikely to survive 90 days
6. Inability to follow the protocol or return for the 90 day follow up
7. Renal dialysis (including hemo or peritoneal dialysis)
We found this trial at
70
sites
Brooklyn, New York 11203
Principal Investigator: Steven Levine, MD
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185 Cambridge Street
Boston, Massachusetts 02114
Boston, Massachusetts 02114
617-724-5200
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6071 West Outer Drive
Detroit, Michigan 48235
Detroit, Michigan 48235
Principal Investigator: Wazim Mohamed, MD
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1200 Moursund Street
Houston, Texas 77030
Houston, Texas 77030
(713) 798-4951
Principal Investigator: Chethan I Rao, MD
Baylor College of Medicine Baylor College of Medicine in Houston, the only private medical school...
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1211 Medical Center Dr
Nashville, Tennessee 37232
Nashville, Tennessee 37232
(615) 322-5000
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Mount Sinai Med Ctr Founded in 1852, The Mount Sinai Hospital is a 1,171-bed, tertiary-care...
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3400 Spruce St
Philadelphia, Pennsylvania 19104
Philadelphia, Pennsylvania 19104
(215) 662-4000
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201 Presidents Circle
Salt Lake City, Utah 84108
Salt Lake City, Utah 84108
801) 581-7200
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1200 Old York Road
Abington, Pennsylvania 19001
Abington, Pennsylvania 19001
(215) 481–2000
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525 E Market St
Akron, Ohio 44304
Akron, Ohio 44304
(330) 375-3000
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500 S State St
Ann Arbor, Michigan 48109
Ann Arbor, Michigan 48109
(734) 764-1817
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1364 Clifton Rd NE
Atlanta, Georgia 30322
Atlanta, Georgia 30322
(404) 712-2000
Principal Investigator: Vishal Patel, MD
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80 Jesse Hill Jr Dr SE
Atlanta, Georgia 30303
Atlanta, Georgia 30303
(404) 616-1000
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University of Maryland Medical Center Founded in 1823 as the Baltimore Infirmary, the University of...
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Charlottesville, Virginia 22903
(434) 924-0311
Principal Investigator: Karen C Johnston, MD, MSc
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251 E Huron St
Chicago, Illinois 60611
Chicago, Illinois 60611
(312) 926-2000
Principal Investigator: Shyam Prabhakaran, MD
Northwestern Memorial Hospital Northwestern Memorial is an academic medical center hospital where the patient comes...
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2600 Clifton Ave
Cincinnati, Ohio 45267
Cincinnati, Ohio 45267
(513) 556-6000
Principal Investigator: Opeolu Adeoye, MD
University of Cincinnati The University of Cincinnati offers students a balance of educational excellence and...
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Dallas, Texas 75390
Principal Investigator: Christiana Hall, MD, MS
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Dallas, Texas 75390
Principal Investigator: Christiana Hall, MD, MS
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Lexington, Kentucky
859) 257-9000
Principal Investigator: Roger L Humphries, MD
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Long Beach, California 90801
Principal Investigator: Nema Ramezan, MD
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Los Angeles, California 90095
Principal Investigator: Sidney Starkman, MD
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Minneapolis, Minnesota 55414
Principal Investigator: Michelle BIROS, MD
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2450 Riverside Ave
Minneapolis, Minnesota 55454
Minneapolis, Minnesota 55454
(612) 273-3000
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Morgantown, West Virginia 26506
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630 W 168th St
New York, New York
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3401 N Broad St
Philadelphia, Pennsylvania
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Principal Investigator: Kendra Drake, MD
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