Unique ID issued by UMIN | UMIN000037106 |
---|---|
Receipt number | R000041679 |
Scientific Title | Clinical study of GLP-1 receptor agonist (Exenatide) for type 2 diabetes patients with diabetic nephropathy |
Date of disclosure of the study information | 2019/06/19 |
Last modified on | 2025/04/22 10:12:29 |
Clinical study of GLP-1 receptor agonist (Exenatide) for type 2 diabetes patients with diabetic nephropathy
Clinical study of exenatide for type 2 diabetes patients with diabetic nephropathy
Clinical study of GLP-1 receptor agonist (Exenatide) for type 2 diabetes patients with diabetic nephropathy
Clinical study of exenatide for type 2 diabetes patients with diabetic nephropathy
Japan |
type 2 diabetes
Endocrinology and Metabolism |
Others
NO
Accumulated cases where single administration of a GLP-1 agonist was administered to type 2 diabetes patients with inadequate glycemic control with diabetic nephropathy, or accumulated cases where the sulfonylurea drug ,thiazolidine drug, biguanide drug, a-glucosidase inhibitor, glinide drug were coadministered, GLP-1 action to investigate the efficacy and safety of the drug's hypoglycemic action and its effect on renal function.
Efficacy
Rate of change of delta eGFR at 12 weeks before and after administration
Interventional
Single arm
Non-randomized
Open -no one is blinded
Self control
1
Treatment
Medicine |
Administer GLP-1 receptor agonist (Exenatide)
1. In principle, this drug is administered within 60 minutes before morning supper and not after meals.
2. The administration of this drug starts with 5 ug once a day, twice a day. After increasing the dose from 5 ug to 10 ug, hypoglycemia and gastrointestinal disorders tend to increase. Therefore, at least one month after the start of administration, follow-up, and in consideration of efficacy and safety, Carefully judge whether to increase the amount to 10 ug at once or twice a day.
20 | years-old | <= |
80 | years-old | > |
Male and Female
Patients with type 2 diabetes who meet the criteria below
1) HbA1c (NGSP): 7.0% or more and less than 10%
2) Patients aged 20 years or older and less than 80 years regardless of gender
3) Diabetic nephropathy stage 2-3 (diagnostic criteria attached)
4) Patients who can obtain written consent to participate in this clinical research
Patients who fall under any of the following are excluded from this clinical study.
1) Patients who fall under the contraindication for GLP-1 receptor agonist
2) Patients participating in other clinical research
3) Pregnant women, pregnant women, lactating women or women who may have pregnancy
4) Patients with other serious complications
5) Patients judged to be unsuitable as a target by the judgment of other doctors
30
1st name | Koji |
Middle name | |
Last name | Murao |
Kagawa University Hospital
Department of Endocrinology and Metabolism
761-0793
Ikenobe 1750-1, Miki-cho, Kita-gun, Kagawa
0878985111
labmed@med.kagawa-u.ac.jp
1st name | Kensaku |
Middle name | |
Last name | Fukunaga |
Kagawa University Hospital
Department of Endocrinology and Metabolism
761-0793
Ikenobe 1750-1, Miki-cho, Kita-gun, Kagawa
0878985111
labmed@med.kagawa-u.ac.jp
Kagawa University
none
Other
Kagawa University of Medicine Ethics Committee
Ikenobe 1750-1, Miki-cho, Kita-gun, Kagawa
0878985111
chiken@med.kagawa-u.ac.jp
NO
2019 | Year | 06 | Month | 19 | Day |
Unpublished
Completed
2015 | Year | 11 | Month | 01 | Day |
2015 | Year | 11 | Month | 01 | Day |
2015 | Year | 12 | Month | 01 | Day |
2020 | Year | 03 | Month | 31 | Day |
2019 | Year | 06 | Month | 19 | Day |
2025 | Year | 04 | Month | 22 | Day |
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000041679