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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT00714324
Other study ID # ELIA003
Secondary ID
Status Recruiting
Phase N/A
First received July 3, 2008
Last updated January 2, 2009
Start date July 2008
Est. completion date July 2009

Study information

Verified date January 2009
Source University of Southampton
Contact Marinos Elia, Professor
Phone 02380 796317
Email elia@soton.ac.uk
Is FDA regulated No
Health authority United Kingdom: Research Ethics Committee
Study type Observational

Clinical Trial Summary

The purpose of this study is to determine if patients are able to reliably screen themselves for nutrition risk.


Recruitment information / eligibility

Status Recruiting
Enrollment 2200
Est. completion date July 2009
Est. primary completion date July 2009
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Male or female

- Adults aged > 18years

- Able to complete screening and provide written informed consent

- Willingness to take part

Exclusion Criteria:

- Children (<18years)

- Pregnant women

- Inpatients

- Unable to complete screen due to physical or mental incapacity

- Unable to comprehend oral and written English language

- Participation in other nutrition studies

Study Design

N/A


Related Conditions & MeSH terms


Locations

Country Name City State
United Kingdom Southampton University Hospitals NHS trust Southampton Hampshire

Sponsors (2)

Lead Sponsor Collaborator
University of Southampton University Hospital Southampton NHS Foundation Trust.

Country where clinical trial is conducted

United Kingdom, 

Outcome

Type Measure Description Time frame Safety issue
Primary To validate the use of a screening tool for patient use 1 year No
Secondary To assess prevalence of malnutrition in outpatients 1 year No
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