UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000035098
Receipt number R000040008
Scientific Title Comparison of real-time vs. professional continuous glucose monitoring related to calibration
Date of disclosure of the study information 2018/12/01
Last modified on 2019/12/02 09:16:42

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Basic information

Public title

Comparison of real-time vs. professional continuous glucose monitoring related to calibration

Acronym

Comparison of real-time vs. professional continuous glucose monitoring related to calibration

Scientific Title

Comparison of real-time vs. professional continuous glucose monitoring related to calibration

Scientific Title:Acronym

Comparison of real-time vs. professional continuous glucose monitoring related to calibration

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 accuracy of real-time and professional continuous glucose monitoring (CGM) by evaluating sensor glucose variability in pre and post of blood glucose levels used to calibrate in real-time and professional CGM

Basic objectives2

Safety,Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

CaI (original index) of each 160 pair in real-time and professional CGM

Key secondary outcomes

Relationship between CaI A (original index) and CaI B (original index) in real-time and professional CGM


Base

Study type

Observational


Study design

Basic design


Randomization


Randomization unit


Blinding


Control


Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms


Purpose of intervention


Type of intervention


Interventions/Control_1


Interventions/Control_2


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

Patients with type 2 diabetes who wear Real-time CGM or professional CGM and whose preprandial and bedtime glucose levels from day 2 to day 5 are evaluated.

Key exclusion criteria

judged to be unsuitable for participation for medical reasons

Target sample size

20


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

0568-62-8111

Email

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


Email

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

Email

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

2018 Year 12 Month 01 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

12

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

2018 Year 12 Month 01 Day

Date of IRB

2018 Year 11 Month 30 Day

Anticipated trial start date

2018 Year 12 Month 01 Day

Last follow-up date

2018 Year 12 Month 31 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information

This is a cross-sectional study. We investigate each 160 pair of blood glucose levels used to calibrate and sensor glucose levels in pre and post of those in 10 patients on real-time CGM and in 10 patients on professional CGM. We evaluate preprandial and bedtime glucose levels from days 2 to 5.


Management information

Registered date

2018 Year 12 Month 01 Day

Last modified on

2019 Year 12 Month 02 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000040008


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name