- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05050851
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
Status
Not yet recruiting
Conditions
Intervention / Treatment
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.
Sponsor
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
Additional Relevant MeSH Terms
- Pathologic Processes
- Metabolic Diseases
- Infections
- Respiratory Tract Infections
- Respiratory Tract Diseases
- Lung Diseases
- Hematologic Diseases
- Blood Protein Disorders
- Anemia, Hypochromic
- Anemia
- Iron Metabolism Disorders
- Hypoproteinemia
- Anemia, Iron-Deficiency
- Pneumonia
- Growth Disorders
- Hypoalbuminemia
Other Study ID Numbers
- AOMSaid
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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