Actively Recruiting

Phase Not Applicable
Age: 18Years - 80Years
All Genders
NCT06801769

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

Age: 18Years - 80Years
All Genders

Eligibility Criteria

Eligible

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.
Not Eligible

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

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

1
2
3
+1

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

Loading map...

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

Not the Right Trial for You?

Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.

Already have an account? Log in here