- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07255989
Diagnosis of Fatty Pancreas by FibroScan (FattyPancreas)
November 27, 2025 updated by: Prof.Reda Mohamed Elbadawy, Benha University
A Study About the Role of Gut Microbiome in Fatty Liver -Fatty Pancreas and Heart Diseases .
Example 2: Interventional study The goal of this observational study is to learn know about the use of FibroScan in diagnosis of fatty pancreas in obese and non obese patients which done for the first time at worldwide as well as Egypt .The participtants already came to do liver FibroScan at center of excellence , Benha University , Egypt.
Untill now the diagnosis of fatty pancreas by MRI which accurate and specific and diagnose fatty pancreasif it is more than 6.2% .
lough the use of abdominal ultrasound also is proved .
The use of digital fibroscan which is easy non invasive , unique as well as we can diagnose fibrosis too in the same sitting .So it is highly recommended to be add with examination of liver by fibroscan.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
This Interventional study done for subjects attend Center of excellence , at Benha University .
aged of patients was from 30 years to 70 years old , both male and females , obese or non and DM or non .
the patients came to do fibroscan to liver .
Lab investigations in the form of CBC ,ESR , liver function tests , kidney function tests.
Complete lipid profile , HbA1c .clincal
and physical examinations done as regard BMI, past history for metabolic diseases , operations and blood transfusion.
FibroScan done first to liver while the patients fastinf at least 3 hours with the know specific position recommendation (banana like ).The position for pancreas examination by fibroScan differe as the patient dorsal position/ recumbancy and his hand behind his head .
take deep breah and slighlty keep it .
some tilting to the left or right . the probe of fibroscan in the epigastrium under the left rib.which totally differe than liver which in the RT anterior axillary line 8 th intercostal space.picture
taken , the unique , novality of this modility is the diagnosis of fibrosis too like liver.Grading of aftty pancreas was done as well as fibrosis of pancreas as follow :S1 =264 dB/m , S2 =276 dB/m and S3 =336 dB/m .
Study Type
Interventional
Enrollment (Actual)
50
Phase
- Not Applicable
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
-
-
Qalyubia Governorate
-
Banhā, Qalyubia Governorate, Egypt, 1531
- Benha University , Egypt
-
-
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
- Adult
- Older Adult
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- Subjects aged from 30 to 70 years old , both male and females , DM or not obese or non obese
Exclusion Criteria:
Exclusion Criteria:
- Subjects with significant amount of alcohol consumption or history of alcohol consumption (>60 g/day).
- History of steatogenic medications (amiodarone, valproic acid, corticosteroids, tetracyclines).
Patients with a previous history of pancreatic disease
-
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
- Primary Purpose: Diagnostic
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: the patients evaluated clinically , physically and interview after that examination done by Fibr
|
In the meeting time abou the nutrition we talk about our ancient egyptian food which confirmed with Carton already present at center of excellence ,
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
prevelance of fatty pancreas 60% which is more common than the expection
Time Frame: 6 months
|
the need to raise uo the importance to use FibroScan to diagnosis of fatty pancreas which is novel , unique and invasive , specific
|
6 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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.
Helpful Links
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 19, 2023
Primary Completion (Actual)
April 19, 2024
Study Completion (Actual)
May 5, 2024
Study Registration Dates
First Submitted
November 17, 2025
First Submitted That Met QC Criteria
November 27, 2025
First Posted (Actual)
December 1, 2025
Study Record Updates
Last Update Posted (Actual)
December 1, 2025
Last Update Submitted That Met QC Criteria
November 27, 2025
Last Verified
November 1, 2025
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- CEPHENo5145,2022,BU.
- Ministry of Higher education (Other Identifier: Benha University)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
IPD Plan Description
because the property of the technique
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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