UMIN-CTR Clinical Trial
| Unique ID issued by UMIN | UMIN000042668 |
|---|---|
| Receipt number | R000048683 |
| Scientific Title | Usability of early treatment intervention using personal CGM in hospitalized patients with type 2 diabetes |
| Date of disclosure of the study information | 2020/12/06 |
| Last modified on | 2022/11/18 09:19:14 |
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Basic information
Public title
Usability of early treatment intervention using personal CGM in hospitalized patients with type 2 diabetes
Acronym
Usability of early treatment intervention using personal CGM in hospitalized patients
Scientific Title
Usability of early treatment intervention using personal CGM in hospitalized patients with type 2 diabetes
Scientific Title:Acronym
Usability of early treatment intervention using personal CGM in hospitalized patients
Region
| Japan |
Condition
Condition
type 2 diabetes
Classification by specialty
| Endocrinology and Metabolism |
Classification by malignancy
Others
Genomic information
NO
Objectives
Narrative objectives1
To investigate usability of early treatment intervention using personal CGM in hospitalized patients with type 2 diabetes
Basic objectives2
Safety,Efficacy
Basic objectives -Others
Trial characteristics_1
Trial characteristics_2
Developmental phase
Assessment
Primary outcomes
Number of days needed to achieve both TIR70-180>70% and CV<36%
Key secondary outcomes
Base
Study type
Interventional
Study design
Basic design
Parallel
Randomization
Randomized
Randomization unit
Individual
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 | Device,equipment |
Interventions/Control_1
This is a randomized parallel-group comparative study. 30 hospitalized patients with type 2 diabetes are randomly allocated to 2 groups. In group 1, patients wear personal CGM and treatment intervention is performed based on the CGM data (CGM group).Treatment intervention is performed at evening from day 2 to day 5 and at morning from day 3 to day 5.
Interventions/Control_2
This is a randomized parallel-group comparative study. 30 hospitalized patients with type 2 diabetes are randomly allocated to 2 groups. In group 2, patients wear professional CGM and treatment intervention is performed based on the glucometer data (BGM group). Treatment intervention is performed at evening from day 2 to day 5 and at morning from day 3 to day 5.
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
| 90 | years-old | > |
Gender
Male and Female
Key inclusion criteria
Hospitalized patients with type 2 diabetes
Key exclusion criteria
Patients whose TIR (70-180) > 70 % and CV < 36 %
judged to be unsuitable for participation for medical reasons
Target sample size
30
Research contact person
Name of lead principal investigator
| 1st name | Soichi |
| Middle name | |
| Last name | Takeishi |
Organization
Inuyama Chuo General Hospital
Division name
Diabetes
Zip code
484-8511
Address
6, Futagozuka, Goromaru, Inuyama-city, Aichi, Japan.
TEL
0568628111
souichi19811225@yahoo.co.jp
Public contact
Name of contact person
| 1st name | Soichi |
| Middle name | |
| Last name | Takeishi |
Organization
Inuyama Chuo General Hospital
Division name
Diabetes
Zip code
484-8511
Address
6, Futagozuka, Goromaru, Inuyama-city, Aichi, Japan.
TEL
0568-62-8111
Homepage URL
souichi19811225@yahoo.co.jp
Sponsor or person
Institute
Inuyama Chuo General Hospital
Institute
Department
Personal name
Funding Source
Organization
Inuyama Chuo General Hospital
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
Inuyama Chuo General Hospital
Address
6, Futagozuka, Goromaru, Inuyama-city, Aichi, Japan.
Tel
0568-62-8111
souichi19811225@yahoo.co.jp
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
Other administrative information
Date of disclosure of the study information
| 2020 | Year | 12 | Month | 06 | 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
| 2020 | Year | 08 | Month | 15 | Day |
Date of IRB
| 2020 | Year | 12 | Month | 04 | Day |
Anticipated trial start date
| 2020 | Year | 12 | Month | 06 | Day |
Last follow-up date
| 2021 | Year | 10 | Month | 31 | Day |
Date of closure to data entry
Date trial data considered complete
Date analysis concluded
Other
Other related information
Management information
Registered date
| 2020 | Year | 12 | Month | 06 | Day |
Last modified on
| 2022 | Year | 11 | Month | 18 | Day |
Link to view the page
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000048683
