- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07768982
Clinical Characteristics and Prognostic Factors in Patients With Meningitis at Sohag Governorate.
August 12, 2026 updated by: Yehia Atef Khalifa Elsayed, Sohag University
Analyze of Clinical Characteristics and Prognostic Factors in Patients With Meningitis at Sohag Governorate
analyze the clinical characteristics and prognostic factors in patients with meningitis at Sohag Governorate .This is an ambidirectional (retrospective and prospective), hospital-based observational study.
The study involves a retrospective review of patient records over the past 3 years, combined with a prospective recruitment of new patients for one year from the initiation of the study
Study Overview
Status
Not yet recruiting
Conditions
Study Type
Observational
Enrollment (Estimated)
300
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: YEHIA ATEF
- Phone Number: 20010333109026
- Email: yehiaatef183@gmail.com
Study Locations
-
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Egypt
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Sohag, Egypt, Egypt, 20
- Sohag Fever Hospital
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Contact:
- يحيي عاطف
-
-
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
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Sampling Method
Non-Probability Sample
Study Population
All patients diagnosed with meningitis and admitted to Sohag Fever Hospital during the study period, regardless of age or sex, who meet the study eligibility criteria.
Description
Inclusion Criteria:
- All patients diagnosed with meningitis admitted to Sohag Fever Hospital during the study period.
- Patients of all age groups and both sexes.
- Patients with confirmed diagnosis based on clinical features and CSF analysis.
Exclusion Criteria:
- Patients with incomplete medical records.
- Patients with uncertain diagnosis of meningitis.
- Patients discharged against medical advice before completion of evaluation.
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 |
|---|---|---|
|
All-cause in-hospital mortality
Time Frame: From hospital admission until hospital discharge, up to 30 days.
|
Death from any cause occurring during hospitalization, reported as the number and percentage of participants who died during hospital admission.
|
From hospital admission until hospital discharge, up to 30 days.
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Recovery without neurological sequelae at hospital discharge
Time Frame: From hospital admission until hospital discharge, up to 30 days.
|
Number and percentage of participants who recover from meningitis without documented neurological sequelae at hospital discharge.
|
From hospital admission until hospital discharge, up to 30 days.
|
|
Neurological sequelae at hospital discharge
Time Frame: From hospital admission until hospital discharge, up to 30 days.
|
Number and percentage of participants with documented neurological sequelae related to meningitis at hospital discharge.
|
From hospital admission until hospital discharge, up to 30 days.
|
|
In-hospital complications
Time Frame: From hospital admission until hospital discharge, up to 30 days.
|
Number and percentage of participants who develop complications during hospitalization, with the type of complication recorded.
|
From hospital admission until hospital discharge, up to 30 days.
|
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 (Estimated)
August 15, 2026
Primary Completion (Estimated)
August 15, 2027
Study Completion (Estimated)
November 15, 2027
Study Registration Dates
First Submitted
August 2, 2026
First Submitted That Met QC Criteria
August 12, 2026
First Posted (Actual)
August 17, 2026
Study Record Updates
Last Update Posted (Actual)
August 17, 2026
Last Update Submitted That Met QC Criteria
August 12, 2026
Last Verified
August 1, 2026
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- Soh-Med-26-7-13MS
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.