UMIN-CTR Clinical Trial
| Unique ID issued by UMIN | UMIN000014179 |
|---|---|
| Receipt number | R000016513 |
| Scientific Title | Required propofol dose and time to emerge for anesthesia; affect by type of neurological disorder |
| Date of disclosure of the study information | 2014/06/05 |
| Last modified on | 2015/01/14 12:26:33 |
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Basic information
Public title
Required propofol dose and time to emerge for anesthesia; affect by type of neurological disorder
Acronym
Required propofol dose and time to emerge for anesthesia
Scientific Title
Required propofol dose and time to emerge for anesthesia; affect by type of neurological disorder
Scientific Title:Acronym
Required propofol dose and time to emerge for anesthesia
Region
| Japan |
Condition
Condition
dental patients with neurological disorder who were treated under intravenous general anesthesia
Classification by specialty
| Dental medicine |
Classification by malignancy
Others
Genomic information
NO
Objectives
Narrative objectives1
We investigated the dose of propofol administered, the time to emerge from intravenous general anesthesia, and the modelled propofol blood concentration at emergence.
Basic objectives2
Pharmacokinetics
Basic objectives -Others
Trial characteristics_1
Trial characteristics_2
Developmental phase
Assessment
Primary outcomes
anesthesia finish
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
| 13 | years-old | <= |
Age-upper limit
| 65 | years-old | >= |
Gender
Male and Female
Key inclusion criteria
patients with neurological disorder who were treated under intravenous general anesthesia at the Dentistry outpatient section for patients with neurological disorder, Kagoshima University Medical Dental Hospital
Key exclusion criteria
The cases that did not use TCI and BIS or did not consent of study were excluded.
Target sample size
200
Research contact person
Name of lead principal investigator
| 1st name | |
| Middle name | |
| Last name | Kentaro Ouchi |
Organization
Kagoshima University Graduate School of Medical and Dental Sciences
Division name
Department of Dental Anesthesiology, Field of Oral and Maxillofacial Rehabilitation,
Zip code
Address
8-35-1 Sakuragaoka, Kagoshima, 890-8544 JAPAN
TEL
099-275-5111
ken2006anes@yahoo.co.jp
Public contact
Name of contact person
| 1st name | |
| Middle name | |
| Last name | Kentaro OUCHI |
Organization
Kagoshima University
Division name
Anesthesia center
Zip code
Address
8-35-1 Sakuragaoka, Kagoshima, 890-8544 JAPAN
TEL
099-275-5111
Homepage URL
ken2006anes@yahoo.co.jp
Sponsor or person
Institute
Department of Dental Anesthesiology, Field of Oral and Maxillofacial Rehabilitation, Kagoshima University Graduate School of Medical and Dental Sciences
Institute
Department
Personal name
Funding Source
Organization
Kagoshima University Graduate School of Medical and Dental Sciences
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
Other administrative information
Date of disclosure of the study information
| 2014 | Year | 06 | Month | 05 | 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
No longer recruiting
Date of protocol fixation
| 2007 | Year | 04 | Month | 01 | Day |
Date of IRB
Anticipated trial start date
| 2007 | Year | 04 | Month | 01 | Day |
Last follow-up date
Date of closure to data entry
Date trial data considered complete
Date analysis concluded
Other
Other related information
propofol dose required for anesthesia, time to emergence, and modelled propofol blood concentration at emergence were evaluated.
Management information
Registered date
| 2014 | Year | 06 | Month | 05 | Day |
Last modified on
| 2015 | Year | 01 | Month | 14 | Day |
Link to view the page
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000016513
