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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT03728400
Other study ID # DENUTRITION USINV
Secondary ID
Status Active, not recruiting
Phase
First received
Last updated
Start date May 29, 2018
Est. completion date December 30, 2023

Study information

Verified date March 2023
Source Groupe Hospitalier Paris Saint Joseph
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This aim of the study is to set up a procedure for screening for undernutrition in the neurovascular intensive care unit. This screening procedure follows a specific work concerning undernutrition in thrombolyzed patients (NCT03303820). This work was motivated by the fact that, despite a high frequency of undernutrition in the hospital (at least 30% of patients), undernutrition in neurovascular unit is studied very little. A cohort of thrombolysed patients in 2014 was studied retrospectively. Patients malnourished at the entrance had a non-significant, less good recovery of their stroke (+ 1 Rankin score point at 3 months in malnourished patients at the entrance).


Description:

The main objective of this project is to assess, prospectively, the frequency of undernutrition at the entrance to the neurovascular intensive care unit and to evaluate the implementation of the undernutrition screening procedure.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 66
Est. completion date December 30, 2023
Est. primary completion date August 30, 2019
Accepts healthy volunteers No
Gender All
Age group 70 Years and older
Eligibility Inclusion Criteria: - Patient whose age = 70 years - Patient hospitalized in Neurovascular Intensive care Unit following a stroke (infarction or cerebral hematoma) - Francophone patient Exclusion Criteria: - Patient hospitalized in Neurovascular Intensive care Unit following a transient ischemic attack - Patient whose age = 70 years - Patient hospitalized in Neurovascular Intensive care Unit for another reason than neurovascular disease - Patient opposing the use of his data

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
France Groupe Hospitalier Paris Saint-Joseph Paris

Sponsors (1)

Lead Sponsor Collaborator
Groupe Hospitalier Paris Saint Joseph

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary frequency of undernutrition at the entrance The primary endpoint is the number of patients who have had an assessment of their nutritional status, that is, for whom undernutrition is detected according to the terms proposed in the undernutrition screening procedure: search for previous quantified weight loss, input BMI, albuminemia. Day 1
Secondary Modified Rankin scale The Rankin score will be performed in post stroke consultation, 3 months after inclusion. Rankin scale: 0 no symptoms, 1 No significant disability. Able to carry out all usual activities, despite some symptoms, 2 Slight disability. Able to look after own affairs without assistance, but unable to carry out all previous activities, 3 Moderate disability. Requires some help, but able to walk unassisted, 4 Moderately severe disability. Unable to attend to own bodily needs without assistance, and unable to walk unassisted, 5 Severe disability. Requires constant nursing care and attention, bedridden, incontinent 3 months
Secondary Recurrence rate of ischemic or haemorrhagic stroke The recurrence of stroke will be collected during the post stroke consultation, 3 months after inclusion. 3 months
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