Trial statusNot yet recruiting
Trial phasePhase 4
Trial typeInterventional
Biological sexAll
Age18-75
SponsorThe Fourth Affiliated Hospital of Zhejiang University School of Medicine
About this trial
To compare the efficacy and safety of the combination of alogliptin and actoplus met with that of actoplus met alone in improving the glucose and lipid metabolism and pancreatic function in T2DM patients complicated with MAFLD.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Clinical diagnosis of T2DM
Clinical diagnosis of MAFLD
HbA1c: 6.5-9.5%
BMI: 19-35 kg/m2
Disqualifiers
Severe infections, surgeries and other emergency
Other types of diabetes
Severe cardiovascular, brain, liver and kidney disorders
Malignant tumor
Trial design
Design model
Parallel
Treatments tested in this trial
alogliptin and actoplus met
Drugcombination of alogliptin and actoplus met
actoplus met
Drugactoplus met
Treatment groups
80 Participants
are divided into 2 treatment groupsGroup A: alogliptin and actoplus metExperimental treatment 1 intervention
Group B: actoplus metActive comparator 1 intervention
Trial outcomes
Primary outcomes
1
hemoglobin A1c
Time frame
6 months of treatmentLocations
Sponsors and contacts
Click on the lead sponsor to view all of their trials.
Source ClinicalTrials.gov
This trial is not recruiting at the moment. You can still explore other options: