- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06727188
Atypical Pneumonia
December 6, 2024 updated by: Aya Gamal hussein, Assiut University
Clinico Laboratory Study of Unresolving Pneumonia in Children
The goal of this observational study is to learn about causes of unresolved pneumonia in children who take appropriate antimicrobial therapy.
Study Overview
Status
Not yet recruiting
Conditions
Intervention / Treatment
Detailed Description
Recurrent pneumonia is defined as two episodes of pneumonia in 1 year or three episodes over any time frame.
Non resolving pneumonias are characterized by the persistence of symptoms and roentgenographic abnormalities for more than 1 month.
The key step in evaluating the patient referred for recurrent or persistent pneumonia is to review the clinical and radiographic features of the episodes to determine if there is adequate documentation to proceed with treatment.
After deciding that a patient has had a persistent episode of pneumonia or the requisite number of recurrent episodes of pneumonia (accompanied by radiographic evidence of pulmonary infiltrates), it is essential to classify the episodes into those involving single or multiple lobes.
On the basis of this classification.
Study Type
Observational
Enrollment (Estimated)
45
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Aya Gamal Hussein, Resident doctor
- Phone Number: 01060617625 800-555-5555
- Email: yoyo74031@gmail.com
Study Locations
-
-
-
Assiut, Egypt
- Pediatrics hospital AssiutUniversity
-
-
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
- Child
Accepts Healthy Volunteers
No
Sampling Method
Non-Probability Sample
Study Population
Children included in the definition of unresolving pneumonia
Description
Inclusion Criteria:
Patients with incomplete resolution by 4 weeks despite appropriate antimicrobial therapy.
- From the age of one month to the age of 6 years old.
Exclusion Criteria:
*Age of the patient below one month and above 6 years old.
- Patients with chronic lung diseases.
- Patients with immunodeficiency.
- Patient with aspiration pneumonia.
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 |
|---|---|---|
|
studying the prevalence of unresolving pneumonia and determining the underlying ateology .
Time Frame: One year
|
Recurrent pneumonia is defined as two episodes of pneumonia in 1 year or three episodes over any time frame.
Non resolving pneumonias are characterized by the persistence of symptoms and roentgenographic abnormalities for more than 1 month.
The key step in evaluating the patient referred for recurrent or persistent pneumonia is to review the clinical and radiographic features of the episodes to determine if there is adequate documentation to proceed with treatment.
After deciding that a patient has had a persistent episode of pneumonia or the requisite number of recurrent episodes of pneumonia (accompanied by radiographic evidence of pulmonary infiltrates), it is essential to classify the episodes into those involving single or multiple lobes.
On the basis of this classification.
|
One year
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Study Director: Maher Mokhtar Ahmed, Professor, AssiutUniversity
- Study Director: Ahlam Badawi Ali, Doctor, AssiutUniversity
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.
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 (Estimated)
January 1, 2025
Primary Completion (Estimated)
January 1, 2025
Study Completion (Estimated)
February 2, 2025
Study Registration Dates
First Submitted
September 7, 2024
First Submitted That Met QC Criteria
December 6, 2024
First Posted (Estimated)
December 10, 2024
Study Record Updates
Last Update Posted (Estimated)
December 10, 2024
Last Update Submitted That Met QC Criteria
December 6, 2024
Last Verified
December 1, 2024
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- Atypical pneumonia
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
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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