Unique ID issued by UMIN | UMIN000004642 |
---|---|
Receipt number | R000005537 |
Scientific Title | Comparison of glycemic control among diabetics using the defferent insulin pen needles. |
Date of disclosure of the study information | 2010/12/01 |
Last modified on | 2012/07/03 19:52:11 |
Comparison of glycemic control among diabetics using the defferent insulin pen needles.
Comparison of glycemic control
Comparison of glycemic control among diabetics using the defferent insulin pen needles.
Comparison of glycemic control
Japan |
Type 1 and 2 diabetes
Endocrinology and Metabolism |
Others
NO
Evaluate efficacy and safety of BD Microfine plus 32G x 4mm Pen Needle by examining whether it provides equivalent glycemic control in diabetic subjects as Novo Pen needle 32G x 6mm by measuring glycated albumin values. Survey patient comfort on this new needle as well.
Safety,Efficacy
Confirmatory
Pragmatic
Not applicable
Average variation rates between glycated albumin level after one-month use of BD Microfine plus 32G x 4mm and that after one-month use of Novo Pen needle 32G x 6mm.
Interventional
Cross-over
Randomized
Individual
Open -no one is blinded
Active
NO
NO
Institution is not considered as adjustment factor.
NO
Pseudo-randomization
2
Treatment
Device,equipment |
Use BD Microfine plus 32G x 4mm for insulin injection during the first 4 weeks and use Novo Pen needle 32G x 6mm during next 4 weeks.
Use Novo Pen needle 32G x 6mm for insulin injection during the first 4 weeks and use BD Microfine plus 32G x 4mm during next 4 weeks.
20 | years-old | <= |
Not applicable |
Male and Female
1)Type 1 and 2 diabetic patients at the age of 20 years or older
2)Insulin-requiring diabetics who have used a pen device for at least one year prior to Study Visit 0
3)Patients who need two or more injections per day.
4)Patients who measure blood glucose level themselves at home.
5)Patients who have maintained a stable Hemoglobin A1C level from 5.5% to 8.5%.
6)Body Mass Index is under 35.
7)Patients who have a will to complete all the procedures of this investigation.
8)Patients who can fill in results on the CRFs.
9)Patients who can understand informed consent and have a will to enroll in this investigation.
1)Pregnancy or possibility of pregnancy.
2)Lactating women
3)Serious neurological diseases
4)Physical conditions which unable subjects to carry out the study procedures (e.g., Incapability to inject by themselves).
5)Thyroid deficiencies and/or nephrotic syndrome.
6)Patients who are currently enrolled in another clinical study
7)Patients who have already discussed details with employees of BD Japan or enrolled study subjects regarding the Investigation.
8)Patients for whom Principle Investigator or Investigators consider that their enrollment could expose them to any risk.
9)Patients who can confuse the interpretation of investigation results or who have done.
10)Employees of pharmaceutical or medical device companies.
40
1st name | |
Middle name | |
Last name | Masato Odawara |
Tokyo Medical University
The 3rd Department of Internal Medicine
160-0023 6-7-1, Shinjuku-ku, Nishi-shinjuku, Tokyo
03-3342-6111
1st name | |
Middle name | |
Last name | Takashi Miwa |
Tokyo Medical University
The 3rd Department of Internal Medicine
160-0023 6-7-1, Shinjuku-ku, Nishi-shinjuku, Tokyo
03-3342-6111
miwa-t@tokyo-med.ac.jp
Tokyo Medical University
The 3rd Department of Internal Medicine
Nippon Becton Dickinson Company, Ltd.
Profit organization
Japan
NO
東京医科大学病院(東京都)/Tokyo Medical University Hospital (Tokyo)
2010 | Year | 12 | Month | 01 | Day |
Unpublished
Completed
2010 | Year | 03 | Month | 25 | Day |
2010 | Year | 10 | Month | 01 | Day |
2011 | Year | 03 | Month | 01 | Day |
2011 | Year | 04 | Month | 01 | Day |
2011 | Year | 04 | Month | 01 | Day |
2011 | Year | 04 | Month | 01 | Day |
2010 | Year | 12 | Month | 01 | Day |
2012 | Year | 07 | Month | 03 | Day |
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000005537