UMIN-CTR Clinical Trial
| Unique ID issued by UMIN | UMIN000025140 |
|---|---|
| Receipt number | R000027508 |
| Scientific Title | Study on influence that difference in fresh gas flow quantity in the general anesthesia gives to desflurane and carbon dioxide absorbent cost |
| Date of disclosure of the study information | 2016/12/04 |
| Last modified on | 2019/10/25 20:22:07 |
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Basic information
Public title
Study on influence that difference in fresh gas flow quantity in the general anesthesia gives to desflurane and carbon dioxide absorbent cost
Acronym
Study on influence that difference in fresh gas flow quantity in the general anesthesia gives to desflurane and carbon dioxide absorbent cost
Scientific Title
Study on influence that difference in fresh gas flow quantity in the general anesthesia gives to desflurane and carbon dioxide absorbent cost
Scientific Title:Acronym
Study on influence that difference in fresh gas flow quantity in the general anesthesia gives to desflurane and carbon dioxide absorbent cost
Region
| Japan |
Condition
Condition
Oto-rhino-laryngologic surgery
Classification by specialty
| Oto-rhino-laryngology |
Classification by malignancy
Others
Genomic information
NO
Objectives
Narrative objectives1
Study on influence that difference in fresh gas flow quantity in the general anesthesia gives to desflurane and carbon dioxide absorbent cost
Basic objectives2
PK,PD
Basic objectives -Others
Trial characteristics_1
Trial characteristics_2
Developmental phase
Assessment
Primary outcomes
Total use time per one soda lime in each group.
Key secondary outcomes
The number of anesthesia that reached with one soda lime.
Consumption of desflurane in each group.
Cost of desflurane in each group.
Base
Study type
Interventional
Study design
Basic design
Parallel
Randomization
Randomized
Randomization unit
Individual
Blinding
Open -no one is blinded
Control
Dose comparison
Stratification
NO
Dynamic allocation
Institution consideration
Blocking
Concealment
Intervention
No. of arms
3
Purpose of intervention
Treatment
Type of intervention
| Medicine |
Interventions/Control_1
1L/min Flesh Gas Flow of the anesthesia maintenance
Interventions/Control_2
1.5L/min Flesh Gas Flow of the anesthesia maintenance
Interventions/Control_3
3L/min Flesh Gas Flow of the anesthesia maintenance
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
A 20 years or older patient whom planned the otolaryngologic operation and operation time is within four hours more than one hour.
Key exclusion criteria
ASA-PS is more than 3
Patient with the past of the malignant hyperthermia
Target sample size
100
Research contact person
Name of lead principal investigator
| 1st name | Hiroshi |
| Middle name | |
| Last name | Morisaki |
Organization
Keio University school of medicine
Division name
Department of anesthesiology
Zip code
1600003
Address
Shinanomachi 35, shinjyuku-ku, Tokyo
TEL
03-3353-1211
t.igarashi.z6@keio.jp
Public contact
Name of contact person
| 1st name | Toru |
| Middle name | |
| Last name | Igarashi |
Organization
Keio University school of medicine
Division name
Department of anesthesiology
Zip code
1600003
Address
Shinanomachi 35, shinjyuku-ku, Tokyo
TEL
03-3353-1211
Homepage URL
t.igarashi.z6@keio.jp
Sponsor or person
Institute
Keio University school of medicine
Institute
Department
Personal name
Funding Source
Organization
Keio University school of medicine
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
Keio University school of medicine
Address
Shinanomachi 35, shinjyuku-ku, Tokyo
Tel
09057985321
eleck216@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
| 2016 | Year | 12 | Month | 04 | 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
70
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
Terminated
Date of protocol fixation
| 2018 | Year | 09 | Month | 01 | Day |
Date of IRB
| 2016 | Year | 12 | Month | 26 | Day |
Anticipated trial start date
| 2017 | Year | 01 | Month | 06 | 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
Management information
Registered date
| 2016 | Year | 12 | Month | 04 | Day |
Last modified on
| 2019 | 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=R000027508
