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Role of Nutrition in Patients Over 75 Years of Age With Stroke (INFRA)

U

University Hospital Center (CHU) Dijon Bourgogne

Status

Completed

Conditions

Stroke

Treatments

Other: completion of a quality of life questionnaire

Study type

Interventional

Funder types

Other

Identifiers

NCT02856009
Béjot 2015

Details and patient eligibility

About

Stroke in elderly subjects has a more severe clinical presentation (in terms of frequency of aphasia, hemiplegia or consciousness disorders), and a worse functional and vital prognosis. Patients older than 75 years also show excess mortality. One of the hypotheses to explain this situation is the high level of frailty in this population. Many tools to measure the concept of frailty have been developed. One important dimension of these tools is the nutritional status. Indeed, protein-energy malnutrition in the elderly, though a frequent situation, is also a complex phenomenon.

The aim of this study is therefore to analyse the impact of protein-energy malnutrition, as a marker of frailty, on the early prognosis (at 28 days) in the aftermath of stroke in subjects older than 75 years hospitalized in Dijon CHU.

Enrollment

177 patients

Sex

All

Ages

75+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients with symptomatic stroke defined according to WHO criteria (including cerebral infarction and intracerebral haemorrhage) managed at the stroke ICU, Neurology 1, Neurology 2, Internal Medicine 2 or Geriatrics at Dijon CHU during the period from 1st November 2015 to 30th September 2016.
  • Patients aged 75 years and older.
  • Patients who have provided informed consent to take part in the study.

Exclusion criteria

  • Patients with meningeal haemorrhage or TIA.
  • Patients who refuse to take part in the study.
  • Patients with hypo-albuminemia not related to malnutrition: chronic infectious or inflammatory syndrome, nephrotic syndrome, exudative enteropathy, hydration disorders.
  • Subjects in custody.
  • Patients (or person of trust) who cannot be contacted by telephone during the follow-up.

Trial design

Primary purpose

Other

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

177 participants in 1 patient group

patient
Experimental group
Treatment:
Other: completion of a quality of life questionnaire

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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