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Clinical Trial Details

Trial ID: L2689
Source ID: NCT01337440
Associated Drug: Udca
Title: Efficacy and Safety of Ursodeoxycholic Acid (UDCA) Added to the DPP-4 Inhibitor in People With Type 2 Diabetes and Chronic Liver Diseases
Acronym:
Status: UNKNOWN
Study Results: NO
Results:
Conditions: Type 2 Diabetes Mellitus|Chronic Liver Disease
Interventions: DRUG: UDCA|DRUG: Sitagliptin
Outcome Measures: Primary: the difference of haemoglobin A1c (HbA1c) and glycoalbumin (GA), the difference of haemoglobin A1c (HbA1c) and glycoalbumin (GA) treating by Ursodeoxycholic Acid (UDCA)or sitagliptin monotherapy, and combination therapy of both two drugs for 3 monthes., 6 months | Secondary: Change from Baseline in Glucagon-like peptide-1 (GLP-1) response to lipid meal test (fat 55%), 6 months|Change from Baseline in energy expenditure, 6months|Change from Baseline in fasting plasma glucose level, 6months|change from baseline in autonomic nerve function, This is performed by power-spectrum analyses of heart rate variability, 6 months
Sponsor/Collaborators: Sponsor: Kanazawa University
Gender: ALL
Age: CHILD, ADULT, OLDER_ADULT
Phases: PHASE4
Enrollment: 20
Study Type: INTERVENTIONAL
Study Designs: Allocation: RANDOMIZED|Intervention Model: PARALLEL|Masking: NONE|Primary Purpose: TREATMENT
Start Date: 2010-04
Completion Date: 2013-03
Results First Posted:
Last Update Posted: 2011-04-18
Locations: Internal medicine, Kanazawa university hospital, Kanazawa, Ishikawa, 920-8641, Japan
URL: https://clinicaltrials.gov/show/NCT01337440