Nutritional Parameters and Other Risk Factors Affecting Severity of Pneumonia in Children Under Five Years in Upper Egypt

September 14, 2021 updated by: Asmaa Omar Mahmoud Said, Assiut University
Decrease mortality rate resulting from pneumonia

Study Overview

Detailed Description

Recruiting patients with pneumonia admitted at Assiut University hospital . Then assessment of their condition and severity of pneumonia by examination and X-ray chest . After that, we aim at assessment their nutrition status and it's effect on severity of pneumonia. So we aim to investigate them by CBC, Albumin, CRP and CXR and correlate these parameters with the severity of pneumonia to assess the impact of nutrition on outcome of chest infections

Study Type

Observational

Enrollment (Anticipated)

30

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

1 month to 5 years (Child)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Probability Sample

Study Population

children admitted at Assiut university children hospital below five years with diagnosis of pneumonia on admission.

Description

Inclusion Criteria:

  • Diagnosis of pneumonia on day 1 of hospital admission.

Exclusion Criteria:

  • patients with cardiac diseases
  • patients with immune deficiency disorders

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

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
ratio of body mass index in patients with pneumonia
Time Frame: Day 1 assessment on hospital admission
we calculate height of patients in metres and weight in Kg then we divide the weight over the height square to get the body mass index
Day 1 assessment on hospital admission

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Concentration of Albumin in patients with pneumonia in g/dl
Time Frame: Day 1 assessment on hospital admission
blood samlpe will be taken for measuring Albumin level
Day 1 assessment on hospital admission
Hemoglobin level in patients with pnemonia in g/dl
Time Frame: Day 1 assessment on hospital admission
blood samlpe will be taken for measuring hemoglobin level
Day 1 assessment on hospital admission

Collaborators and Investigators

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

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 (Anticipated)

September 30, 2021

Primary Completion (Anticipated)

April 30, 2022

Study Completion (Anticipated)

October 30, 2022

Study Registration Dates

First Submitted

September 21, 2020

First Submitted That Met QC Criteria

September 14, 2021

First Posted (Actual)

September 21, 2021

Study Record Updates

Last Update Posted (Actual)

September 21, 2021

Last Update Submitted That Met QC Criteria

September 14, 2021

Last Verified

September 1, 2021

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

IPD Plan Description

No identifiable data will be available to others apart from me as data collector

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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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