UMIN-CTR Clinical Trial

BACK TOP
UMIN-CTR English Home Glossary (Simple) FAQ Search clinical trials

Name:
UMIN ID:

Recruitment status
Unique ID issued by UMIN UMIN000024711
Receipt No. R000028430
Scientific Title Difference of presepsin in blood specimen separation
Date of disclosure of the study information 2016/11/04
Last modified on 2016/11/04

* This page includes information on clinical trials registered in UMIN clinical trial registed system.
* We don't aim to advertise certain products or treatments


Basic information
Public title Difference of presepsin in blood specimen separation
Acronym Difference of presepsin in blood specimen separation
Scientific Title Difference of presepsin in blood specimen separation
Scientific Title:Acronym Difference of presepsin in blood specimen separation
Region
Japan

Condition
Condition Patients of sepsis without renal failure
Classification by specialty
Emergency medicine Intensive care medicine Not applicable
Adult
Classification by malignancy Others
Genomic information NO

Objectives
Narrative objectives1 Investigation of a difference between whole blood and plasma in presepsin measurement.
Basic objectives2 Others
Basic objectives -Others Decision of which the blood condition is good for presepsin measurement.
Trial characteristics_1 Confirmatory
Trial characteristics_2 Explanatory
Developmental phase Not applicable

Assessment
Primary outcomes Measurement of presepsin in condition of whole blood and plasma.
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
20 years-old <=
Age-upper limit

Not applicable
Gender Male and Female
Key inclusion criteria The patients of sepsis or expected sepsis without renal failure.
Key exclusion criteria renal failure
Target sample size 30

Research contact person
Name of lead principal investigator
1st name
Middle name
Last name Maki Kida
Organization Wakayama Medical University
Division name Department of Emergency and Crotical Care
Zip code
Address 811-1, Kimiidera, Wakayama
TEL 073-447-2300
Email shinop@wamayama-med.ac.jp

Public contact
Name of contact person
1st name
Middle name
Last name Maki Kida
Organization Wakayama Medical University
Division name Department of Emergency and Crotical Care
Zip code
Address 811-1, Kimiidera, Wakayama
TEL 073-447-2300
Homepage URL
Email shinop@wamayama-med.ac.jp

Sponsor
Institute Wakayama Medical University, Department of Emergency and Crotical Care
Institute
Department

Funding Source
Organization Wakayama Medical University, Department of Emergency and Crotical Care
Organization
Division
Category of Funding Organization Local Government
Nationality of Funding Organization

Other related organizations
Co-sponsor
Name of secondary funder(s)

IRB Contact (For public release)
Organization
Address
Tel
Email

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 和歌山県立医科大学

Other administrative information
Date of disclosure of the study information
2016 Year 11 Month 04 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
Date of protocol fixation
2014 Year 09 Month 15 Day
Date of IRB
Anticipated trial start date
2014 Year 09 Month 15 Day
Last follow-up date
Date of closure to data entry
Date trial data considered complete
Date analysis concluded

Other
Other related information It is an observation study.

Management information
Registered date
2016 Year 11 Month 04 Day
Last modified on
2016 Year 11 Month 04 Day


Link to view the page
URL(English) https://upload.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000028430

Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name


Contact us.