Because the aim of this observational study is to obtain insight in the nutrient and fluid intake, and nutrient and biomarker concentrations in the blood in patients with ischemic stroke, the focus will be on descriptive statistics and there will be…
ID
Bron
Verkorte titel
Aandoening
Ischemic stroke
Ondersteuning
Onderzoeksproduct en/of interventie
Uitkomstmaten
Primaire uitkomstmaten
- Nutrient and fluid intake over time<br>
- Biomarkers of vitamin and mineral status over time<br>
- (Risk of) malnutrition
Achtergrond van het onderzoek
This observational, longitudinal study is designed to learn more about the nutritional status of patients with an ischemic stroke during hospitalization immediately after stroke incidence and during rehabilitation in the first months after hospital discharge.
Doel van het onderzoek
Because the aim of this observational study is to obtain insight in the nutrient and fluid intake, and nutrient and biomarker concentrations in the blood in patients with ischemic stroke, the focus will be on descriptive statistics and there will be no study hypothesis.
Onderzoeksopzet
hospital admission, hospital admission + 1 day, hospital discharge (day of discharge or day 8), hospital admission + 6 weeks, hospital admission + 13 weeks
Onderzoeksproduct en/of interventie
No intervention
Publiek
PO Box 80141
Monique Visser
Utrecht 3508 TC
The Netherlands
+31 30 2095 000
Monique.Visser@danone.com
Wetenschappelijk
PO Box 80141
Monique Visser
Utrecht 3508 TC
The Netherlands
+31 30 2095 000
Monique.Visser@danone.com
Belangrijkste voorwaarden om deel te mogen nemen (Inclusiecriteria)
- Age ≥ 50 and ≤ 80 years
- Diagnosis of ischemic stroke
- Included for participation in the study within 24h after admission.
Belangrijkste redenen om niet deel te kunnen nemen (Exclusiecriteria)
- History of progressive neurological disorders (e.g. Parkinson¡¯s disease, dementia, multiple sclerosis).
- Receiving any cancer treatment within 1 year before entry into the study (signing of informed consent).
- Blood donation or receiving blood transfusion within 4 weeks before entry into the study (informed consent) and/or planned blood donation during the study
- Diagnosis of haemorrhagic stroke (subarachnoid or intracerebral) or transient ischemic attack at hospital admission
- Traumatic brain injury
- Any medical condition that significantly interferes with digestion and/or gastrointestinal (GI) function except for dysphagia (e.g. short bowel syndrome, inflammatory bowel disease, gastric ulcer, gastritis (gastro)enteritis, GI cancer) as judged by the investigator.
Opzet
Deelname
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Andere (mogelijk minder actuele) registraties in dit register
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In overige registers
| Register | ID |
|---|---|
| NTR-new | NL6795 |
| NTR-old | NTR6981 |
| Ander register | Nutricia Research : 16R&07575 |