UMIN-CTR Clinical Trial
| Unique ID issued by UMIN | UMIN000025271 |
|---|---|
| Receipt number | R000029063 |
| Scientific Title | Perioperative Characteristics of the Accuracy of Subcutaneous Continuous Glucose Monitoring |
| Date of disclosure of the study information | 2016/12/16 |
| Last modified on | 2019/11/17 14:12:00 |
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Basic information
Public title
Perioperative Characteristics of the Accuracy
of Subcutaneous Continuous Glucose Monitoring
Acronym
Perioperative Characteristics of the Accuracy
of Subcutaneous Continuous Glucose Monitoring
Scientific Title
Perioperative Characteristics of the Accuracy
of Subcutaneous Continuous Glucose Monitoring
Scientific Title:Acronym
Perioperative Characteristics of the Accuracy
of Subcutaneous Continuous Glucose Monitoring
Region
| Japan |
Condition
Condition
Patients who were scheduled to undergo neurological, plastic, otorhinolaryngologic cardiac surgery
Classification by specialty
| Anesthesiology | Adult |
Classification by malignancy
Others
Genomic information
NO
Objectives
Narrative objectives1
To investigate the correlation between blood glucose level and interstitial glucose level using subcutaneous continuous glucose monitoring system during the intraoperative period.
Basic objectives2
Safety,Efficacy
Basic objectives -Others
Trial characteristics_1
Trial characteristics_2
Developmental phase
Assessment
Primary outcomes
Correlation between blood glucose level and interstitial glucose level
Key secondary outcomes
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
| Not applicable |
Gender
Male and Female
Key inclusion criteria
Patients aged 20 years or older who is planned intraoperative arterial pressure monitoring
Key exclusion criteria
N/A
Target sample size
60
Research contact person
Name of lead principal investigator
| 1st name | Ryo |
| Middle name | |
| Last name | Wakabayashi |
Organization
Shinshu University Hospital
Division name
Department of Anesthesiology and Resuscitology
Zip code
390-8621
Address
3-1-1, Asahi, Matsumoto-shi, Nagano
TEL
0263-37-2670
waka0924@shinshu-u.ac.jp
Public contact
Name of contact person
| 1st name | Ryo |
| Middle name | |
| Last name | Wakabayashi |
Organization
Shinshu University Hospital
Division name
Department of Anesthesiology and Resuscitology
Zip code
390-8621
Address
3-1-1, Asahi, Matsumoto-shi, Nagano
TEL
0263-37-2670
Homepage URL
waka0924@shinshu-u.ac.jp
Sponsor or person
Institute
Department of Anesthesiology and Resuscitology, Shinshu University Hospital
Institute
Department
Personal name
Funding Source
Organization
Department of Anesthesiology and Resuscitology, Shinshu University Hospital
Organization
Division
Category of Funding Organization
Other
Nationality of Funding Organization
Other related organizations
Co-sponsor
Name of secondary funder(s)
IRB Contact (For public release)
Organization
Shinshu University Certified Review Board of Clinical Research
Address
3-1-1, Asahi, Matsumoto-shi, Nagano
Tel
0263-37-2572
mdrinri@shinshu-u.ac.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
| 2016 | Year | 12 | Month | 16 | 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 | 12 | Month | 06 | Day |
Date of IRB
| 2016 | Year | 12 | Month | 08 | Day |
Anticipated trial start date
| 2016 | Year | 12 | Month | 16 | Day |
Last follow-up date
| 2017 | Year | 10 | Month | 31 | Day |
Date of closure to data entry
Date trial data considered complete
Date analysis concluded
Other
Other related information
Subcutaneous sensor was inserted into the patient's upper arm, and we investigated the intraoperative correlation between blood glucose level and interstitial glucose level using subcutaneous continuous glucose monitoring system.
Management information
Registered date
| 2016 | Year | 12 | Month | 14 | Day |
Last modified on
| 2019 | Year | 11 | Month | 17 | Day |
Link to view the page
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000029063
