Actively Recruiting
Study for the Identification of a Score to Assess Intrapancreatic Fat Through Eco-Elastography and Its Correlation With Metabolic Syndrome and Insulin-Secreting Cells.
Led by Catholic University of the Sacred Heart · Updated on 2026-03-20
100
Participants Needed
2
Research Sites
89 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
\*\*Brief Summary of the SPES Clinical Study\*\* The SPES clinical study aims to evaluate the relationship between pancreatic fat accumulation (pancreatic steatosis) and metabolic health. Pancreatic steatosis has been linked to conditions like type 2 diabetes (T2D) and metabolic syndrome, but the underlying mechanisms and its impact on beta-cell function remain poorly understood. The primary goal of this study is to develop a quantitative ultrasound elastography score to measure the degree of pancreatic steatosis and explore how this relates to pancreatic beta-cell function and key factors associated with the development of type 2 diabetes and metabolic syndrome. A secondary goal is to categorize participants into four risk classes for type 2 diabetes based on their metabolic profiles and correlate these classes with the degree of pancreatic steatosis. This may provide insights into individual risk stratification for T2D and related complications. The study will enroll 100 participants, aged 18 to 80, attending the Endoscopic Ultrasound Unit at the Fondazione Policlinico Universitario Agostino Gemelli in Rome. Participants will undergo endoscopic ultrasound for various clinical reasons, excluding those with pancreatic tumors, cystic fibrosis, or insulin-treated diabetes. Key inclusion criteria include controlled blood glucose levels (HbA1c \< 10% or fasting glucose \< 250 mg/dL) and the ability to understand and provide informed consent. The study is interventional but does not involve drugs or medical devices. Participants will attend a visit where medical history, physical measurements (e.g., BMI, waist circumference, blood pressure), glucose tolerance tests, and blood work will be collected. This comprehensive approach aims to better understand the metabolic implications of pancreatic steatosis and its role in type 2 diabetes development. The study will last 24 months, including the enrollment period. Findings may contribute to improved risk stratification, prevention, and management strategies for type 2 diabetes and related conditions.
CONDITIONS
Official Title
Study for the Identification of a Score to Assess Intrapancreatic Fat Through Eco-Elastography and Its Correlation With Metabolic Syndrome and Insulin-Secreting Cells.
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age between 18 and 80 years
- HbA1c less than 10% or fasting glucose less than 250 mg/dL
- Ability to understand and provide informed consent regarding the procedures, data collection, and analysis.
You will not qualify if you...
- Age under 18 years or over 80 years
- History of diabetes treated with insulin
- HbA1c greater than 10% or fasting glucose greater than 250 mg/dL
- Pancreatic diseases including solid tumors, secretory neuroendocrine tumors, cystic fibrosis; non-secretory NETs and IPMN may be included
- Previous pancreatic surgery
- Moderate anemia with hemoglobin less than 10 mg/dL
- Severe liver failure classified as Child-Pugh C
- Non-metabolic causes of non-alcoholic fatty liver disease such as certain medications, hemochromatosis, malnutrition, or infections like HBV/HIV
- Alcohol abuse exceeding 30 grams per day of ethanol
- Pregnancy and breastfeeding
- Inability to adequately understand informed consent and study procedures
AI-Screening
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Trial Site Locations
Total: 2 locations
1
Gemelli University Hospistal
Rome, Lazio, Italy, 00168
Actively Recruiting
2
Gemelli University Hospital
Rome, Lazio, Italy, 00168
Actively Recruiting
Research Team
T
Teresa Mezza
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
DIAGNOSTIC
Number of Arms
1
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