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Main
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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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ClinicalTrials.gov |
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Last refreshed on:
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12 December 2020 |
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Main ID: |
NCT02664376 |
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Date of registration:
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19/01/2016 |
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Prospective Registration:
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No |
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Primary sponsor: |
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Public title:
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Prevalence of Sarcopenia and Its Geriatric Features
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Scientific title:
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Prevalence of Sarcopenia and Its Geriatric Features |
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Date of first enrolment:
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January 1, 2016 |
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Target sample size:
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834 |
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Recruitment status: |
Completed |
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URL:
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https://clinicaltrials.gov/show/NCT02664376 |
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Study type:
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Observational |
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Study design:
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Phase:
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Countries of recruitment
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Belgium
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Contacts
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Name:
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Marie Claessens, MD |
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Address:
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Telephone:
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Email:
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Affiliation:
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CHU Brugmann |
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Name:
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Robin Barré, MD |
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Address:
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Telephone:
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Email:
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Affiliation:
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CHU Brugmann |
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Name:
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Florence Benoît, MD |
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Address:
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Telephone:
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Email:
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Affiliation:
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CHU Brugmann |
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Name:
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Murielle Surquin, MD |
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Address:
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Telephone:
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Email:
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Affiliation:
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CHU Brugmann |
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- To be admitted in the unit 83 of the Geriatric Departement of the CHU Brugmann
hospital, from 10/01/2016 till 30/03/2017.
Exclusion Criteria:
- Patients unable to consent or without representatives
- Patients unable to perform the hand- grip test, the walk test or measurement of the
body components by DEXA
- Patients in severe pain
- Bedridden patients
- Patients for which a clear therapeutic abstention has been established
- Language barriere that cannot be overcome
- Patients unable to walk without the help of a third person
Age minimum:
65 Years
Age maximum:
N/A
Gender:
All
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Health Condition(s) or Problem(s) studied
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Sarcopenia
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Intervention(s)
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Other: Sarcopenia detection
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Primary Outcome(s)
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Prevalence of sarcopenia
[Time Frame: From 10/01/2016 till 30/03/2017 (up to 15 months)]
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Secondary Outcome(s)
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Percentage of hospitalized patients unable to perform the sarcopenia detection test
[Time Frame: From 10/01/2016 till 30/03/2017 (up to 15 months)]
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Secondary ID(s)
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CHUB-sarcopenia
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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Results
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Results available:
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Date Posted:
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Date Completed:
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URL:
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