Management Concepts of Metabolic Dysfunction Associated Steatotic Liver Disease (MASLD) Among Chinese Physicians

ConditionLiver Disease
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorNovo Nordisk A/S

About this trial

This study is a cross-sectional survey-based study. The main goal of this study is to investigate the attitudes, perceptions, and clinical practice in assessing liver fibrosis following a metabolic dysfunction-associated steatotic liver disease (MASLD) diagnosis, and the management of MASLD patients among Chinese physicians in the departments of endocrinology / hepatology / infection / gastroenterology in Grade IIIA hospitals in provincial capitals or municipalities.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Has provided informed consent.

Registered clinical practice location in provincial capital or municipality.

Physician with a license for clinical practice.

Employed in the Department of Endocrinology, Hepatology, Infection or Gastroenterology.

Disqualifiers

None

Trial population

Physicians from department of endocrinology, hepatology, gastroenterology, department of infectious diseases, and from Grade IIIA hospitals located in provincial capitals will be enrolled to take the survey.

Trial design

Design model

Other

Time perspective

Cross-sectional

Treatments tested in this trial

  • No treatment is given

    Other intervention

    This study is a cross-sectional survey-based study. The design is observational and descriptive. Collection of data will be performed via a quantitative online survey.

Treatment groups

470 Participants
are divided into 1 treatment group
Group A: Physicians treating MASLD1 intervention

Trial outcomes

Primary outcomes

1

To investigate attitudes and perceptions concerning the reasons for further severity assessment (mainly refers to the assessment of liver fibrosis) following a MASLD diagnosis

The reason for severity assessment will be measured via questionnaires. The corresponding questionnaire items were designed to explore whether physicians would conduct further evaluation for patients diagnosed with MASLD and what dimensions such further evaluation would cover. Details of the questions are shown below: 1. For patients with confirmed MASLD, will you perform additional diagnostic evaluation? (Single choice) * Yes, I will conduct subsequent assessment and risk stratification * No, a confirmed MASLD diagnosis is sufficient. 2. For physicians who selected "Yes": What dimensions will your additional diagnostic evaluation cover? (Multiple choices) * Rule out other liver diseases * Assess metabolic comorbidities and risk factors * Identify whether the patient has concurrent MASH * Determine the stage of liver fibrosis * Others, please specify

Time frame
At the data capture (Day 1)
2

Methods used for diagnose liver fibrosis

Methods used for liver fibrosis diagnosis will be assessed via questionnaires. The corresponding questionnaire items asked physicians to select the examinations they use to assess the stage of liver fibrosis in patients with MASLD. For physicians who perform liver fibrosis staging: Among patients with confirmed MASLD, which of the following tools do you use in routine clinical practice to evaluate liver fibrosis stage? Available response options include FibroScan, FibroTouch, Magnetic Resonance Elastography (MRE), fibrosis-specific serological tests (e.g., PIIINP, C-IV, LN, HA), simple scoring systems (e.g., FIB-4, NFS, APRI), and others (please specify).

Time frame
At the data capture (Day 1)
3

To find percentages of patients who undergo different liver fibrosis examination

Percentages of patients who undergo different liver fibrosis examination will be measured via questionnaires. The corresponding questionnaire items asked physicians to report the proportion of patients with MASLD for whom they utilize each liver fibrosis assessment method in routine clinical practice. For each selected examination tool, physicians report the proportion of patients receiving the test in their daily clinical work using predefined categories (≤10%, 10%-25%, 25%-50%, 50%-75%, and 75%-100%).

Time frame
At the data capture (Day 1)
4

To find reasons for insufficient liver fibrosis assessment

This will be assessed via questionnaires. The corresponding questionnaire items investigate whether physicians believe there is insufficient liver fibrosis assessment in current clinical practice. Those who answer affirmatively are then asked to select contributing factors. For patients with confirmed MASLD, physicians are asked: do you think liver fibrosis assessment is currently inadequate in clinical practice? If yes, what are the leading causes of insufficient fibrosis evaluation? Physicians can select from predefined causes, including clinicians paying insufficient attention to liver fibrosis evaluation, low patient acceptance rate of liver biopsy, low diagnostic accuracy of existing noninvasive fibrosis assessment tools, lack of effective pharmacotherapies for liver fibrosis, and others (please specify). There is also an option indicating that there is no inadequate liver fibrosis assessment in clinical practice, which is mutually exclusive with the other options.

Time frame
At the data capture (Day 1)

Secondary outcomes

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.