CompletedPhase 1/2

GSP as an Novel Indicator for Residual Liver Function in Patients With Fatty Liver

210 participantsStarted 2007-07-05

Plain-language summary

The primary objective is to determine the galactose single point (GSP) cutoff values to discriminate subjects with different hepatic function. The secondary objective is to analyze the correlations between GSP and other hepatic function assessment methods among this trial subjects.

Who can participate

Age range20 Years – 80 Years

SexALL

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Inclusion criteria

✓. Male or female with age between 20-80.
✓. Ability and willingness to provide informed consent, adhere to the study visit schedule and complete all study assessments and language specific questionnaires.

Exclusion criteria

✕. History of serious allergic reaction to galactose and have galactosemia.
✕. History of receiving total gastrectomy, subtotal gastrectomy, celiac disease, or small intestinal resection.
✕. History of diabetes mellitus.
✕. Subjects are children or handicapped people.
✕. Subjects with any other reasons considered by the investigator not in the condition to enter into the trial.

What they're measuring

Blood concentration of galactose

Timeframe: Sixty minutes

Trial details

NCT IDNCT04546022

SponsorNational Defense Medical Center, Taiwan

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2007-08-12

View on ClinicalTrials.gov More Galactose Single Point (GSP), Residual Liver Function trials