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NCT06720766Completed

Assessment of FibbroScan in Diagnosing MASLD Among the Chinese Population With Obesity

Source: ClinicalTrials.gov · Last updated 1 Oct 2026

Brief summary (registry, in English)

The non-invasive evaluation of liver steatosis and fibrosis with FibroScan is a routinely procedure in clinical practice for people with obesity. However, there are still considerable uncertainties regarding the potential influence of confounding factors and the optimal application of cut-off values for obesity. The goal of this observational study is to learn about the optimal application of cut-off values of for Chinese people with obesity.

Status (registry)
Completed
Study type
Observational
Enrollment
565 (actual)
First submitted
27 Nov 2024
Start date
24 Oct 2023
Primary completion date
30 Sept 2025
Lead sponsor
The Third People's Hospital of Chengdu
NCT number
NCT06720766

What you commit to

  • Study type: Observational
  • Participants enrolled: 565
  • From 24 Oct 2023 to the primary completion date, 30 Sept 2025
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Patients who have undergone liver transplantation

Other illness

  • Patients with cardiac failure and/or significant valvular disease
  • Patients with a confirmed diagnosis of active malignancy, or other terminal disease

Other

  • Patients with ascites or pregnant women
  • Patients with any active implantable medical device (such as a pacemaker or defibrillator)
  • Patients with haemochromatosis
  • Patients who have refused to undergo LB or blood tests
  • Patients participating in another clinical trial within the preceding 30 days

Who the study is looking for

  • Patients aged 18 years or older who provided written informed consent
  • Patients who schedule to undergo bariatric surgery and a liver biopsy (LB) for the investigation of suspected MASLD
  • Patients who schedule to undergo FibroScan examination

Age in the registry: 18 years to 70 years · Sex: All

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
The Third People's Hospital of Chengdu
Coordinator of this site? Confirm its status
ChengduChinaUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.