UMIN-CTR Clinical Trial
| Unique ID issued by UMIN | UMIN000042084 |
|---|---|
| Receipt number | R000048026 |
| Scientific Title | Volatile anesthetics concentration in blood during cardio pulmonary bypass |
| Date of disclosure of the study information | 2020/10/27 |
| Last modified on | 2023/10/14 09:57:39 |
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Basic information
Public title
Volatile anesthetics concentration in blood during cardio pulmonary bypass
Acronym
Volatile anesthetics concentration in blood during cardio pulmonary bypass
Scientific Title
Volatile anesthetics concentration in blood during cardio pulmonary bypass
Scientific Title:Acronym
Volatile anesthetics concentration in blood during cardio pulmonary bypass
Region
| Japan |
Condition
Condition
Cardiovascular surgery
Classification by specialty
| Anesthesiology | Cardiovascular surgery | Adult |
Classification by malignancy
Others
Genomic information
NO
Objectives
Narrative objectives1
Volatile anesthetic concentration in blood during CPB
Basic objectives2
Pharmacokinetics
Basic objectives -Others
Trial characteristics_1
Trial characteristics_2
Developmental phase
Assessment
Primary outcomes
Volatile anesthetic concentration in blood during CPB
Key secondary outcomes
Measuring desflurane concentration in blood during CPB
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
Cardiac surgery for over 20-year-old-patinets
Non criteria for gender, age, height and body weight.
Informed consent before the research
Key exclusion criteria
Cases in which it is difficult to continue the research at the discretion of the surgeon or anesthesiologist
Patients who are considered unfit by the study director or co-investigator to participate in this study
Target sample size
200
Research contact person
Name of lead principal investigator
| 1st name | Takahiro |
| Middle name | |
| Last name | Tamura |
Organization
Nagoya University Hospital
Division name
Anesthesiology
Zip code
466-8550
Address
Nagoya
TEL
0527412111
takahiro@med.nagoya-u.ac.jp
Public contact
Name of contact person
| 1st name | Tamura |
| Middle name | |
| Last name | Takahiro |
Organization
Nagoya University Hospital
Division name
Anesthesiology
Zip code
466-8550
Address
Showa-ku
TEL
0527412111
Homepage URL
takahiro@med.nagoya-u.ac.jp
Sponsor or person
Institute
Nagoya University Hospital, Anesthesiology
Institute
Department
Personal name
Funding Source
Organization
Nagoya University Hospital, Anesthesiology
Organization
Division
Category of Funding Organization
Other
Nationality of Funding Organization
Japan
Other related organizations
Co-sponsor
Name of secondary funder(s)
IRB Contact (For public release)
Organization
IRB, Nagoya University hospital
Address
Nagoya
Tel
0527412111
ethics@med.nagoya-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
| 2020 | Year | 10 | Month | 27 | 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 | 10 | Month | 28 | Day |
Date of IRB
| 2020 | Year | 12 | Month | 11 | Day |
Anticipated trial start date
| 2020 | Year | 11 | Month | 15 | Day |
Last follow-up date
| 2023 | Year | 12 | Month | 31 | Day |
Date of closure to data entry
Date trial data considered complete
Date analysis concluded
Other
Other related information
The blood concentration of inhalation anesthetic gas in the heart-lung machine will be measured, and the transition will be examined.
Management information
Registered date
| 2020 | Year | 10 | Month | 12 | Day |
Last modified on
| 2023 | Year | 10 | Month | 14 | Day |
Link to view the page
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000048026
| Research Plan | |
|---|---|
| Registered date | File name |
| Research case data specifications | |
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| Registered date | File name |
| Research case data | |
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| Registered date | File name |
