Unique ID issued by UMIN | UMIN000011218 |
---|---|
Receipt number | R000011698 |
Scientific Title | The effectiveness of Cholestimide on dyslipidemia with visceral fat accumulation in patients with type 2 diabetes. A randomized parallel crossover trial |
Date of disclosure of the study information | 2013/07/18 |
Last modified on | 2014/01/27 12:13:46 |
The effectiveness of Cholestimide
on dyslipidemia with visceral fat accumulation in patients with type 2 diabetes. A randomized parallel crossover trial
The effectiveness of Cholestimide
on dyslipidemia with visceral fat accumulation in patients with type 2 diabetes. A randomized parallel crossover trial
The effectiveness of Cholestimide
on dyslipidemia with visceral fat accumulation in patients with type 2 diabetes. A randomized parallel crossover trial
The effectiveness of Cholestimide
on dyslipidemia with visceral fat accumulation in patients with type 2 diabetes. A randomized parallel crossover trial
Japan |
Type 2 Diabetes, Dyslipidemia
Endocrinology and Metabolism |
Others
NO
To examine the effectiveness of cholestimide on visceral fat, basal metablic rate and blood glucose in type 2 Diabetes, dyslipidemia patients with visceral fat accumulation
Efficacy
Confirmatory
Pragmatic
Not applicable
Visceral fat area
1. Resting energy expenditure, Respiratory quotient
2. HbA1c, blood glucose, Insulin secretion
3.lipid metabolism
4.oxidative stress
Interventional
Cross-over
Randomized
Individual
Open -no one is blinded
Active
NO
NO
NO
Pseudo-randomization
2
Treatment
Medicine |
Administration of Cholestimide 3g/day add on to statin for the first 24 weeks, then withdrawal of Cholestimide for the next 24 weeks
Administration of statin for the first 24 weeks, then add Cholestimide 3g/day for the next 24 weeks
20 | years-old | <= |
70 | years-old | >= |
Male and Female
Patients whose body mass index(BMI) is above 25, Visceral fat area is above 100cm2, andHbA1c(NGSP) is above 6.5%
Patients who have dyslipidemia and administered by Atorvastatin , Pitavastatin or Rosuvastation at least for 2 months, and LDL-cholesterol is above 90 mg/dl
Patients with complete biliary obstruction
Patients with hypersensitivity to cholestimide or past history of ileus.
Patients with poor control of constipation
Patients who take warfarin, tetracycline, Phenobarbital, thyroid gland preparation, digitalis
Patients with unstable proliferative diabetic retinopathy
Patients whose stage of diabetic nephropathy is above stage 4
Patients who have active infection or are under treatment of malignancy
Patients who have macroangiopathy
Patients who are considered to be inadequate to participate in this study.
30
1st name | |
Middle name | |
Last name | Yasuko Uchigata |
Tokyo Women's Medical University
Diabetes Center
8-1 Kawadacho, Shinjuku-ku, Tokyo, Japan
03-3353-8111
uchigata@dmc.twmu.ac.jp
1st name | |
Middle name | |
Last name | Risa Ide |
Tokyo Women's Medical University
Diabetes Center
8-1 Kawadacho, Shinjuku-ku, Tokyo, Japan
03-3353-8111
fujimaki@dmc.twmu.ac.jp
Tokyo Women's Medical University, Diabetes Center
None
Self funding
NO
東京女子医科大学病院(東京都)
2013 | Year | 07 | Month | 18 | Day |
Unpublished
Completed
2007 | Year | 12 | Month | 18 | Day |
2008 | Year | 05 | Month | 01 | Day |
2013 | Year | 09 | Month | 07 | Day |
2013 | Year | 10 | Month | 30 | Day |
2013 | Year | 07 | Month | 18 | Day |
2014 | Year | 01 | Month | 27 | Day |
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000011698