Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
PHASE2/PHASE3
125 participants
INTERVENTIONAL
2005-05-31
2008-06-30
Brief Summary
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Detailed Description
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Before the inclusion started we decided to use the percentage of patients with weight loss ≥ 5 % at 3 months follow-up as the primary outcome measure because this is correlated better to clinical outcomes as e.g. mortality and comorbidity. Secondary outcome measures were then defined as handgrip strength, quality of life, nutritional status, nutrient intake and length of hospital stay.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
NONE
Interventions
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Nutritional support
Eligibility Criteria
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Inclusion Criteria
* 18 years old and above
* \< 7 days since debut of stroke symptoms and either body mass index (BMI) = or \< 20
* Weight loss \> 5% in 3-6 months or there has been little or is likely to be no or very little nutritional intake for \> 5 days
Exclusion Criteria
* Severe dementia
* Reduced consciousness
* Immobility
* Expected short-time survival
18 Years
ALL
No
Sponsors
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University of Oslo
OTHER
Ostfold Hospital Trust
OTHER
Principal Investigators
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Truls Hauge, PhD
Role: STUDY_CHAIR
Ullevaal University Hospital
Locations
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Ostfold Hospital Trust
Fredrikstad, , Norway
Countries
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References
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Ha L, Hauge T, Iversen PO. Body composition in older acute stroke patients after treatment with individualized, nutritional supplementation while in hospital. BMC Geriatr. 2010 Oct 18;10:75. doi: 10.1186/1471-2318-10-75.
Ha L, Hauge T, Spenning AB, Iversen PO. Individual, nutritional support prevents undernutrition, increases muscle strength and improves QoL among elderly at nutritional risk hospitalized for acute stroke: a randomized, controlled trial. Clin Nutr. 2010 Oct;29(5):567-73. doi: 10.1016/j.clnu.2010.01.011. Epub 2010 Feb 21.
Other Identifiers
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297
Identifier Type: -
Identifier Source: org_study_id
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