Clinical trial Recruiting at 1 site Observational Ages 18 and up

MASLD care: how Chinese physicians diagnose and manage liver disease

Official title: Attitudes, Perceptions, Clinical Practice, and Barriers in Diagnosis and Management of Patients With Metabolic Dysfunction-associated Steatotic Liver Disease: a Cross-sectional Survey on Physicians in China

Run by Novo Nordisk A/S · NCT07682363 · Data updated 2026-11-12

This survey asks Chinese doctors in major hospitals how they diagnose, assess fibrosis, and manage MASLD in patients with liver disease.

More Non-Alcoholic Fatty Liver Disease trials

Quick facts

Study typeObservational
Ages18 Years and up
SexAll
Enrollment470 (estimated)
SponsorNovo Nordisk A/S
Industry-sponsored
Locations1 site (Beijing)
StatusRecruiting
StartedJune 3, 2026
Main results expectedFebruary 23, 2027
Study endsFebruary 23, 2027
Registry record updatedJuly 2, 2026
Trial IDNCT07682363 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Physicians licensed to practice, with associate chief or senior attending status, who work in endocrinology, hepatology, infection, or gastroenterology, conduct outpatient clinics, and manage MASLD/MASH patients in Grade IIIA hospitals in provincial capitals or municipalities.

Probably not a fit

Participants may not receive personal benefit; the study only collects professional practices and opinions.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This is a cross-sectional survey of physicians across endocrinology, hepatology, infection, and gastroenterology in Grade IIIA hospitals in provincial capitals or municipalities. It collects attitudes, perceptions, and current clinical practices following MASLD diagnosis, focusing on fibrosis assessment and management strategies. No interventions or treatments are given; the study analyzes responses from clinicians to understand real-world patterns. Participation requires informed consent and meeting specific clinical and practice criteria. The study is sponsored by Novo Nordisk A/S with the Beijing investigational site as the location.

Why it matters

Potential benefit: The findings could inform how MASLD is managed in Chinese hospitals and identify gaps between guidelines and practice.

How similar studies have gone: Similar cross-sectional surveys have helped map physician practices in MASLD care in other regions, supporting the value of this approach.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* 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.
* Hospital level: Grade IIIA hospital.
* Hold a professional title of associate chief physician or above, or senior attending physician (as an attending physician for more than or equal to (≥) 3 years).
* Conducts outpatient clinics for at least 1 half-days per week.
* The patient load of MASLD/MASH per month in the department should be:
* a. Endocrinology ≥20 patients per month
* b. Hepatology/Gastroenterology/ Infectious ≥30 patients per month

Exclusion Criteria:

-Participants will be excluded if they have unwillingness precluding adequate cooperation, fail to complete the questionnaire, or submit questionnaires verified as invalid.

Where it's running

  • Novo Nordisk Investigational site
    Beijing, China
    Recruiting

Study contacts

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.