UMIN-CTR Clinical Trial
| Unique ID issued by UMIN | UMIN000034353 |
|---|---|
| Receipt number | R000032505 |
| Scientific Title | Effect of dulaglutide versus liraglutide on glucose variability and oxidative stress and endothelial function in type 2 diabetes patients |
| Date of disclosure of the study information | 2018/10/10 |
| Last modified on | 2018/10/25 09:10:25 |
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Basic information
Public title
Effect of dulaglutide versus liraglutide on glucose variability and oxidative stress and endothelial function in type 2 diabetes patients
Acronym
Effect of dulaglutide versus liraglutide on glucose variability and oxidative stress and endothelial function in type 2 diabetes patients
Scientific Title
Effect of dulaglutide versus liraglutide on glucose variability and oxidative stress and endothelial function in type 2 diabetes patients
Scientific Title:Acronym
Effect of dulaglutide versus liraglutide on glucose variability and oxidative stress and endothelial function in type 2 diabetes patients
Region
| Japan |
Condition
Condition
Type 2 diabetes mellitus
Classification by specialty
| Endocrinology and Metabolism |
Classification by malignancy
Others
Genomic information
NO
Objectives
Narrative objectives1
we aimed to investigate the effects of from once-weekly dulaglutide to once-daily liraglutide for 24 weeks on oxidative stress, endothelial function
Basic objectives2
Efficacy
Basic objectives -Others
Trial characteristics_1
Trial characteristics_2
Developmental phase
Assessment
Primary outcomes
1)oxidative stress
2)vascular endothelial function
Key secondary outcomes
1)glucose variability
2)DTSQ and eating behavior
3)Fasting plasma glucose,HbA1c
4)TG,HDL-C,LDL-C
5)Systolic and diastolic blood pressure
6)weight
Base
Study type
Interventional
Study design
Basic design
Parallel
Randomization
Randomized
Randomization unit
Cluster
Blinding
Open -no one is blinded
Control
Active
Stratification
Dynamic allocation
Institution consideration
Blocking
Concealment
Intervention
No. of arms
2
Purpose of intervention
Treatment
Type of intervention
| Medicine |
Interventions/Control_1
Dulaglutide
Interventions/Control_2
liragulitide
Interventions/Control_3
Interventions/Control_4
Interventions/Control_5
Interventions/Control_6
Interventions/Control_7
Interventions/Control_8
Interventions/Control_9
Interventions/Control_10
Eligibility
Age-lower limit
| 20 | years-old | <= |
Age-upper limit
| Not applicable |
Gender
Male and Female
Key inclusion criteria
1)a diagnosis of type 2 diabetes mellitus
2)20 years and over
3)HbA1c 6.5% or more
4)treatment with liraglutide for 12weeks or longer
Key exclusion criteria
1)the use of steroids or anti-inflammatory drugs,
2)diabetic ketosis and coma within 3 months before the study,
3)severe infection, severe trauma, pre-and post-operation,
4)an estimated glomerular filtration rate are within 30mL/min/1.73m2,
5)severe liver dysfunction,
6)malignancy,
7)pregnancy
8)Patients who are judged as inappropriate for inclusion by phsicians
Target sample size
50
Research contact person
Name of lead principal investigator
| 1st name | |
| Middle name | |
| Last name | Makoto Ohara |
Organization
Showa University School of Medicine
Division name
Division of Diabetes and Endocrinology, Department of Internal Medicine
Zip code
Address
1-5-8 Hatanodai, Shinagawa-ku, Tokyo
TEL
03-3784-8000
s6018@nms.ac.jp
Public contact
Name of contact person
| 1st name | |
| Middle name | |
| Last name | Makoto Ohara |
Organization
Showa University School of Medicine
Division name
Division of Diabetes and Endocrinology, Department of Internal Medicine
Zip code
Address
1-5-8 Hatanodai, Shinagawa-ku, Tokyo
TEL
03-3784-8000
Homepage URL
s6018@nms.ac.jp
Sponsor or person
Institute
Showa University School of Medicine, Division of Diabetes and Endocrinology, Department of Internal Medicine
Institute
Department
Personal name
Funding Source
Organization
Showa University School of Medicine, Division of Diabetes and Endocrinology, Department of Internal Medicine
Organization
Division
Category of Funding Organization
Self funding
Nationality of Funding Organization
Other related organizations
Co-sponsor
Name of secondary funder(s)
IRB Contact (For public release)
Organization
Address
Tel
Secondary IDs
Secondary IDs
NO
Study ID_1
Org. issuing International ID_1
Study ID_2
Org. issuing International ID_2
IND to MHLW
Institutions
Institutions
昭和大学病院
Other administrative information
Date of disclosure of the study information
| 2018 | Year | 10 | Month | 10 | Day |
Related information
URL releasing protocol
Publication of results
Unpublished
Result
URL related to results and publications
Number of participants that the trial has enrolled
Results
Results date posted
Results Delayed
Results Delay Reason
Date of the first journal publication of results
Baseline Characteristics
Participant flow
Adverse events
Outcome measures
Plan to share IPD
IPD sharing Plan description
Progress
Recruitment status
Completed
Date of protocol fixation
| 2016 | Year | 11 | Month | 28 | Day |
Date of IRB
Anticipated trial start date
| 2016 | Year | 12 | Month | 01 | Day |
Last follow-up date
| 2018 | Year | 03 | Month | 31 | Day |
Date of closure to data entry
| 2018 | Year | 03 | Month | 31 | Day |
Date trial data considered complete
| 2018 | Year | 03 | Month | 31 | Day |
Date analysis concluded
| 2018 | Year | 10 | Month | 01 | Day |
Other
Other related information
Management information
Registered date
| 2018 | Year | 10 | Month | 01 | Day |
Last modified on
| 2018 | Year | 10 | Month | 25 | Day |
Link to view the page
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000032505
