Prospective Study to Quantify the Change in Weight at a Pneumonia (PneumoniePoids)

June 1, 2018 updated by: University Hospital, Grenoble

This study is based on the change in weight of hospitalized patients knowing that the diagnosis of malnutrition based on the presence of at least one clinical or laboratory test which anthropometric measures (Evaluation of diagnostic protein energy malnutrition in hospitalized adults ANAES , Guidelines Department, September 2003; HAS Strategy supported in cases of wasting energy and protein in the elderly April 2007).

The goal of this study is to find the correlation between hospitalization and weight loss, significant risk factors for malnutrition in a situation of community-acquired pneumonia infection.

Study Overview

Status

Unknown

Intervention / Treatment

Study Type

Observational

Enrollment (Anticipated)

188

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Grenoble, France, 38043
        • Recruiting
        • University Hospital Grenoble
        • Contact:
          • Sophie LUMALE, dietician
          • Phone Number: 0476766442

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

Patients with pneumonia.

Description

Inclusion Criteria:

  • cough
  • Fever > 38.5 ° C
  • Tachycardia > 100 / Min
  • Chest pain lateralized
  • Absence of infection high respiratory tract
  • Global Impression of Severity
  • Fireplace auscultatory signs (rattle crackling)

Exclusion Criteria:

  • Pregnant women
  • Dialysis patients
  • Any patient with home oxygen or under a home care for BPCO stage 3 or 4
  • Patients transferred from intensive care
  • Patients with severe sepsis and requiring a "filler"
  • Enteral or parenteral nutrition

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
patients with pneumonia

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Weight history
Time Frame: Few minutes
The weight of the patient, and weight's history.
Few minutes
Standard biology
Time Frame: Few hours
C-reactive protein, Albumine, Transthyretin, Oxygen
Few hours
Severity of pneumonia
Time Frame: Few minutes
Fine's score or CURB 65
Few minutes
The functional status
Time Frame: Few minutes
ADL score ; activities daily living
Few minutes

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

April 1, 2015

Primary Completion (Anticipated)

April 1, 2019

Study Completion (Anticipated)

December 1, 2019

Study Registration Dates

First Submitted

July 11, 2016

First Submitted That Met QC Criteria

July 22, 2016

First Posted (Estimate)

July 26, 2016

Study Record Updates

Last Update Posted (Actual)

June 4, 2018

Last Update Submitted That Met QC Criteria

June 1, 2018

Last Verified

June 1, 2018

More Information

Terms related to this study

Other Study ID Numbers

  • 38RC14.323

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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