UMIN-CTR Clinical Trial
| Unique ID issued by UMIN | UMIN000056145 |
|---|---|
| Receipt number | R000063528 |
| Scientific Title | Comparison of complications associated with noradrenaline administered into central venous catheters and peripheral venous access: a scoping review. |
| Date of disclosure of the study information | 2024/11/13 |
| Last modified on | 2024/11/13 14:52:00 |
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Basic information
Public title
Comparison of complications associated with noradrenaline administered into central venous catheters and peripheral venous access: a scoping review.
Acronym
Comparison of complications associated with noradrenaline administered into CVCs and PiVCs: a ScR.
Scientific Title
Comparison of complications associated with noradrenaline administered into central venous catheters and peripheral venous access: a scoping review.
Scientific Title:Acronym
Comparison of complications associated with noradrenaline administered into CVCs and PiVCs: a ScR.
Region
| Japan |
Condition
Condition
Shock
Classification by specialty
| Emergency medicine |
Classification by malignancy
Others
Genomic information
NO
Objectives
Narrative objectives1
The aim of this study is to systematically map and compare what is known in the existing literature regarding the early and late complications of peripherally versus centrally administered noradrenaline.
Basic objectives2
Safety,Efficacy
Basic objectives -Others
Trial characteristics_1
Trial characteristics_2
Developmental phase
Assessment
Primary outcomes
Early and late complications of noradrenaline administered via peripheral and central venous catheters and related existing research findings
Key secondary outcomes
Base
Study type
Others,meta-analysis etc
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
| Not applicable |
Age-upper limit
| Not applicable |
Gender
Male and Female
Key inclusion criteria
A literature search of Pubmed, Medline, the Cochrane Library, Web of science, and CINAHL will be used to identify literature regarding peripheral versus central venous administration of noradrenaline and norepinephrine and complications.
Key exclusion criteria
The candidates that came up from each search site were some that had been tested on animals, some that were administered via routes other than intravenous administration, and some that were being evaluated in combination with other drugs.
Target sample size
Research contact person
Name of lead principal investigator
| 1st name | Yutaka |
| Middle name | |
| Last name | Kumaido |
Organization
Saitama Medical Center, Jichi Medical University
Division name
Department of Emergency and Critical Care Medicine
Zip code
330-0834
Address
1-847 Amanuma-cho, Omiya-ku, Saitama-shi, Saitama-ken, Japan
TEL
+81-48-647-2111
kumaido.yutaka@jichi.ac.jp
Public contact
Name of contact person
| 1st name | Yutaka |
| Middle name | |
| Last name | Kumaido |
Organization
Saitama Medical Center, Jichi Medical University
Division name
Department of Emergency and Critical Care Medicine
Zip code
330-0834
Address
1-847 Amanuma-cho, Omiya-ku, Saitama-shi, Saitama-ken, Japan
TEL
+81-48-647-2111
Homepage URL
kumaido.yutaka@jichi.ac.jp
Sponsor or person
Institute
Other
Institute
Department
Personal name
Yutaka Kumaido
Funding Source
Organization
Other
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
Saitama Medical Center, Jichi Medical University
Address
1-847 Amanuma-cho, Omiya-ku, Saitama-shi, Saitama-ken, Japan
Tel
+81-48-647-2111
kumaido.yutaka@jichi.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
| 2024 | Year | 11 | Month | 13 | 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
4099
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
| 2024 | Year | 09 | Month | 19 | Day |
Date of IRB
| 2024 | Year | 09 | Month | 19 | Day |
Anticipated trial start date
| 2024 | Year | 09 | Month | 19 | Day |
Last follow-up date
| 2025 | Year | 03 | Month | 30 | Day |
Date of closure to data entry
Date trial data considered complete
Date analysis concluded
Other
Other related information
None
Management information
Registered date
| 2024 | Year | 11 | Month | 13 | Day |
Last modified on
| 2024 | Year | 11 | Month | 13 | Day |
Link to view the page
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000063528
