UMIN-CTR Clinical Trial

Basic information
Public title	L-carnitine level in adult critically ill patients
Acronym	L-carnitine measurement in adult study
Scientific Title	L-carnitine level in adult critically ill patients
Scientific Title:Acronym	L-carnitine measurement in adult study
Region	Japan

Condition
Condition	Adult Critically Ill Patients
Classification by specialty	Emergency medicine Intensive care medicine
Classification by malignancy	Others
Genomic information	NO

Objectives
Narrative objectives1	L-carnitine is vital for lipid metabolism in the body, but yet it is not forlmulated in commercial nutritional formulas. This study reveals the L-catnitine levels for critically ill adults under enteral or parenteral feeding.
Basic objectives2	Others
Basic objectives -Others	Only data collection
Trial characteristics_1
Trial characteristics_2
Developmental phase

Assessment
Primary outcomes	L-carnitine level in Critically ill Adults
Key secondary outcomes

Base
Study type	Observational

Study design
Basic design
Randomization
Randomization unit
Blinding
Control
Stratification
Dynamic allocation
Institution consideration
Blocking
Concealment

Intervention
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Purpose of intervention
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Eligibility
Age-lower limit	18 years-old <=
Age-upper limit	Not applicable
Gender	Male and Female
Key inclusion criteria	Critically ill adult under artificial feed in the ICU
Key exclusion criteria	younger than18years old, pregnancy, elective operation, complicated metabolic disorder
Target sample size	100

Research contact person
Name of lead principal investigator	1st name Middle name Last name Shigeto Oda
Organization	Chiba University Graduate School of Medicine
Division name	Dept. of Emergency and Critical Care Medicine
Zip code
Address	1-8-1 Inohana Chuou-ku, Chiba City
TEL	043-222-7171
Email	odas@faculty.chiba-u.jp

Public contact
Name of contact person	1st name Middle name Last name Taku Oshima
Organization	Chiba University Graduate School of Medicine
Division name	Department of Emergency and Critical Care Medicine
Zip code
Address	1-8-1 Inohana Chuou-ku, Chiba City
TEL	043-222-7171
Homepage URL
Email	t_oshima@chiba-u.jp

Sponsor
Institute	Chiba University Graduate School of Medicine
Institute
Department

Funding Source
Organization	Self funding
Organization
Division
Category of Funding Organization	Self funding
Nationality of Funding Organization

Other related organizations
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IRB Contact (For public release)
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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 03 Month 06 Day

Related information
URL releasing protocol
Publication of results	Published

Result
URL related to results and publications	https://rrtjournal.biomedcentral.com/articles/10.1186/s41100-018-0158-7
Number of participants that the trial has enrolled
Results
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Results Delayed
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Baseline Characteristics
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IPD sharing Plan description

Progress
Recruitment status	Main results already published
Date of protocol fixation	2014 Year 01 Month 31 Day
Date of IRB
Anticipated trial start date	2014 Year 02 Month 03 Day
Last follow-up date	2014 Year 07 Month 31 Day
Date of closure to data entry	2014 Year 07 Month 31 Day
Date trial data considered complete	2014 Year 07 Month 31 Day
Date analysis concluded	2015 Year 08 Month 15 Day

Other
Other related information	Collecting excess serum from enrolled patient's routine blood tests. Completed.

Management information
Registered date	2014 Year 03 Month 06 Day
Last modified on	2018 Year 07 Month 25 Day

Link to view the page
URL(English)	https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000015457

Research Plan
Registered date	File name

Research case data specifications
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Research case data
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