Development and Validation of a Multi-target, Blood-based NAFLD Diagnosis Test (NCT05108415) | Clinical Trial Compass
UnknownNot Applicable
Development and Validation of a Multi-target, Blood-based NAFLD Diagnosis Test
1,500 participantsStarted 2023-05
Plain-language summary
Multi-omics approach was used to identify patterns of serological biomarkers to diagnose NAFLD. The purpose of this study is to develop and validate a blood-based assay to diagnose NAFLD by collecting blood sample from healthy patients undergoing routine screening ultrasonography and from patients recently diagnosed with NAFLD.
Who can participate
Age range20 Years – 85 Years
SexALL
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
COHORT A
Inclusion Criteria:
* 20-85 years of age
* Recently completed ultrasonography examination.
* Recently diagnosed with (or strong clinical suspicion for) primary NAFLD.
* At least 7 days before but no more than 2 months after the most recent ultrasonography
* Able and willing to provide blood samples per protocol
* Able to comprehend and willing to sign and date the written informed consent document(s) and any applicable medical record release documents for the study
Exclusion Criteria:
* Alcohol abuse (weekly ethanol consumption: \>140 g for men and \>70 g for women) in the past year.
* Personal history of NAFLD (other than most recent diagnosis)
* Ultrasonography within the previous 9 years (other than most recent diagnosis)
* A history of fatty liver or other liver diseases such as autoimmune hepatitis and drug-induced liver disease.
* Have a medical condition which, in the opinion of the investigator, should preclude enrollment into the study.
* Have participated or be currently participating in a clinical research study in which an experimental medication has been administered during the 60 days up to and including the date of providing informed consent or may be administered through the time of the ultrasonography.
* If female, known to be pregnant.
COHORT B
Inclusion Criteria:
* 20-85 years of age
* Planning to undergo a screening ultrasonography within 2 months after providing signed informed consent
* Able and willing to provide blood samples per protoc…
What they're measuring
1
Confirmative of Number of Participants with NAFLD Diagnosis