Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT06838988

Ultrasonographic Patterns and Pathological Correlation in the Diagnosis of Subcutaneous Nodules

Led by Mahidol University · Updated on 2025-05-09

100

Participants Needed

1

Research Sites

44 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The objective of this study is to explore the role of ultrasonography (non-invasive imaging device) in the diagnosis of subcutaneous nodules (mass/bumb underneath the skin). Patients who presented with subcutaneous nodules and was indicated for diagnostic skin biopsies were recruited. Prior to skin biopsies (not part of the study's intervention), ultrasonography(intervention) was used to examine the characteristics of the nodules. The ultrasonographic findings are then compared to the pathological results to explore the role of ultrasonography in differentiating each disease or group of diseases that presented with skin nodules.

CONDITIONS

Official Title

Ultrasonographic Patterns and Pathological Correlation in the Diagnosis of Subcutaneous Nodules

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients aged 18 years and older who presented with subcutaneous nodules
  • Indicated for pathological examination for disease diagnosis
  • Subcutaneous nodules located in areas accessible for tissue sampling down to the fat layer
  • Patients who agree to participate by signing the consent form
Not Eligible

You will not qualify if you...

  • Presence of inflammation or other tumors mimicking panniculitis, such as painful lipomas, cellulitis, or leg interstitial edema
  • Diseases significantly altering skin or subcutaneous tissue structure, like scleroderma or severe edema
  • History of previous treatments in the area of the subcutaneous mass (e.g., surgery, radiation, high-dose steroids) that may affect ultrasound results
  • Lesions located on the head or mucous membranes
  • Pregnant or breastfeeding patients
  • Presence of wounds or open sores in the ultrasound examination area
  • History of blood clotting disorders (coagulopathy)
  • Metal implants in the area of interest interfering with ultrasound imaging
  • Participants who refuse or withdraw from the study

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Ramathibodi Hospital

Bangkok, Ratchathewi, Thailand, 10400

Actively Recruiting

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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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