UMIN-CTR Clinical Trial
| Unique ID issued by UMIN | UMIN000011430 |
|---|---|
| Receipt number | R000013382 |
| Scientific Title | Patient's factors influenced on propofol blood concentrations when using target controlled infusion system(DiprifusorTM) |
| Date of disclosure of the study information | 2013/08/10 |
| Last modified on | 2013/12/19 22:03:22 |
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Basic information
Public title
Patient's factors influenced on propofol blood concentrations when using target controlled infusion system(DiprifusorTM)
Acronym
Patient's factors influenced on propofol blood concentrations
Scientific Title
Patient's factors influenced on propofol blood concentrations when using target controlled infusion system(DiprifusorTM)
Scientific Title:Acronym
Patient's factors influenced on propofol blood concentrations
Region
| Japan |
Condition
Condition
Patients scheduled for general anesthesia
Classification by specialty
| Anesthesiology |
Classification by malignancy
Others
Genomic information
NO
Objectives
Narrative objectives1
Investigating patient's factor influenced on propofol blood concentrations when using target contorolled infusion system(Diprifusor TM)
Basic objectives2
Pharmacokinetics
Basic objectives -Others
Trial characteristics_1
Trial characteristics_2
Developmental phase
Assessment
Primary outcomes
Measured blood propofol concentrations
Key secondary outcomes
Base
Study type
Interventional
Study design
Basic design
Single arm
Randomization
Randomized
Randomization unit
Blinding
Open -no one is blinded
Control
Uncontrolled
Stratification
Dynamic allocation
Institution consideration
Blocking
Concealment
Intervention
No. of arms
1
Purpose of intervention
Treatment
Type of intervention
| Medicine |
Interventions/Control_1
Propofol infusion is injected intravenously with target controlled infusion system.
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
| 65 | years-old | >= |
Gender
Male and Female
Key inclusion criteria
Patients scheduled for elective surgery under general anesthesia.
Key exclusion criteria
Drug or alcohol abuse, and hepatic or renal impairment.
Target sample size
100
Research contact person
Name of lead principal investigator
| 1st name | |
| Middle name | |
| Last name | Michiaki Yamakage |
Organization
Sapporo medical university school of medicine
Division name
Department of anesthesiolofy
Zip code
Address
S1W16, chuo-ku, Sapporo, Japan
TEL
011-611-2111
yamakage@sapmed.ac.jp
Public contact
Name of contact person
| 1st name | |
| Middle name | |
| Last name | Yukitoshi Niiyama |
Organization
Sapporo medical university school of medicine
Division name
Department of anesthesiology
Zip code
Address
S1W16, chuo-ku, Sapporo, Japan
TEL
011-611-2111
Homepage URL
niiyama@sapmed.ac.jp
Sponsor or person
Institute
Sapporo mecdical university school of medicine
Institute
Department
Personal name
Funding Source
Organization
nothing
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
Address
Tel
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
札幌医科大学麻酔科学講座
Other administrative information
Date of disclosure of the study information
| 2013 | Year | 08 | Month | 10 | 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
Open public recruiting
Date of protocol fixation
| 2013 | Year | 08 | Month | 01 | Day |
Date of IRB
Anticipated trial start date
| 2013 | Year | 08 | Month | 10 | Day |
Last follow-up date
Date of closure to data entry
Date trial data considered complete
Date analysis concluded
Other
Other related information
Management information
Registered date
| 2013 | Year | 08 | Month | 08 | Day |
Last modified on
| 2013 | Year | 12 | Month | 19 | Day |
Link to view the page
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000013382
