UMIN-CTR Clinical Trial
| Unique ID issued by UMIN | UMIN000041345 |
|---|---|
| Receipt number | R000047058 |
| Scientific Title | Comparison of continuous infusion rate and blood concentration of rocurnium to maintain moderate and deep neuromuscular block between young and elderly surgical patients. |
| Date of disclosure of the study information | 2020/08/08 |
| Last modified on | 2020/08/07 09:34:53 |
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Basic information
Public title
Comparison of continuous infusion rate and blood concentration of rocurnium to maintain moderate and deep neuromuscular block between young and elderly surgical patients.
Acronym
Comparison of continuous infusion rate and blood concentration of rocurnium to maintain moderate and deep neuromuscular block between young and elderly surgical patients.
Scientific Title
Comparison of continuous infusion rate and blood concentration of rocurnium to maintain moderate and deep neuromuscular block between young and elderly surgical patients.
Scientific Title:Acronym
Comparison of continuous infusion rate and blood concentration of rocurnium to maintain moderate and deep neuromuscular block between young and elderly surgical patients.
Region
| Japan |
Condition
Condition
Patients receiving general anesthesia
Classification by specialty
| Anesthesiology |
Classification by malignancy
Others
Genomic information
NO
Objectives
Narrative objectives1
To compare the infusion rate of rocuronium to maintain moderate and deep neuromuscular block between young and elderly surgical patients.
Basic objectives2
PK,PD
Basic objectives -Others
Trial characteristics_1
Trial characteristics_2
Developmental phase
Assessment
Primary outcomes
Infusion rate of rocuronium to maintain moderate neuromuscular block
Key secondary outcomes
Base
Study type
Interventional
Study design
Basic design
Parallel
Randomization
Non-randomized
Randomization unit
Blinding
Open -no one is blinded
Control
Dose comparison
Stratification
Dynamic allocation
Institution consideration
Blocking
Concealment
Intervention
No. of arms
2
Purpose of intervention
Treatment
Type of intervention
| Other |
Interventions/Control_1
elderly patients
Interventions/Control_2
young patients
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
age over 20 and below 45 or age over 70
ASA-PS= 1-3
Key exclusion criteria
patient who is allergic to muscle relaxants
patient who has neuromuscular diseases
patient who has moderate to severe liver function failure
patient who is receiving hemodialysis
Target sample size
60
Research contact person
Name of lead principal investigator
| 1st name | Hajime |
| Middle name | |
| Last name | Iwasaki |
Organization
Nihon University School of Medicine
Division name
Department of Anesthesiology
Zip code
1738610
Address
30-1, Oyaguchi Kamicho, Itabashi-Ku, Tokyo, Japan
TEL
+81-3-3972-8111
iwasaki.hajime@nihon-u.ac.jp
Public contact
Name of contact person
| 1st name | Hajime |
| Middle name | |
| Last name | Iwasaki |
Organization
Nihon University School of Medicine
Division name
Department of Anesthesiology
Zip code
1738610
Address
+81-3-3972-8111
TEL
+81-3-3972-8111
Homepage URL
iwasaki.hajime@nihon-u.ac.jp
Sponsor or person
Institute
Nihon University School of Medicine
Institute
Department
Personal name
Funding Source
Organization
Nihon University School of Medicine
Organization
Division
Category of Funding Organization
Self funding
Nationality of Funding Organization
Other related organizations
Co-sponsor
Name of secondary funder(s)
IRB Contact (For public release)
Organization
Nihon University Itabashi Hospital, Clinical Research Judging Committee
Address
30-1, Oyaguchi Kamicho, Itabashi-Ku, Tokyo, Japan
Tel
+81-3-3972-8111
komoda.nozomi@nihon-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
日本大学医学部付属板橋病院（東京都）
Other administrative information
Date of disclosure of the study information
| 2020 | Year | 08 | Month | 08 | 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
Preinitiation
Date of protocol fixation
| 2020 | Year | 06 | Month | 01 | Day |
Date of IRB
| 2020 | Year | 07 | Month | 17 | Day |
Anticipated trial start date
| 2020 | Year | 08 | Month | 15 | Day |
Last follow-up date
| 2023 | Year | 07 | Month | 01 | Day |
Date of closure to data entry
Date trial data considered complete
Date analysis concluded
Other
Other related information
Management information
Registered date
| 2020 | Year | 08 | Month | 07 | Day |
Last modified on
| 2020 | Year | 08 | Month | 07 | Day |
Link to view the page
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000047058
