UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000022711
Receipt number R000026070
Scientific Title Identifying postoperative delirium by a quick, systemic method-" the nursing delirium screening scale"
Date of disclosure of the study information 2016/06/12
Last modified on 2016/06/12 23:46:02

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Basic information

Public title

Identifying postoperative delirium by a quick, systemic method-" the nursing delirium screening scale"

Acronym

Identifying POD IN NuDESC

Scientific Title

Identifying postoperative delirium by a quick, systemic method-" the nursing delirium screening scale"

Scientific Title:Acronym

Identifying POD IN NuDESC

Region

Asia(except Japan)


Condition

Condition

the incidence of POD was underestimated

Classification by specialty

Anesthesiology

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

to increasing the diagnosis rate of postoperative delirium

Basic objectives2

Others

Basic objectives -Others

to improve the patient safety

Trial characteristics_1

Confirmatory

Trial characteristics_2

Pragmatic

Developmental phase

Not applicable


Assessment

Primary outcomes

to elevate the medical care person's willing to detect the postoperative delirium

Key secondary outcomes

to emphasize the importance of postoperative delirium and the convenient of NuDESC


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

90 years-old >=

Gender

Male and Female

Key inclusion criteria

adult patients receiving general anesthesia and postoperative patient control analgesia

Key exclusion criteria

preoperative psychological diasease,
cardiac surgery, patient can not communicate

Target sample size

2000


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Chen jenyin

Organization

Chi Mei Medical Center

Division name

anesthesiology department

Zip code


Address

No.901, Zhonghua Rd., Yongkang Dist., Tainan City 710, Taiwan (R.O.C.)

TEL

(06)281-2811-53321

Email

chenjenyin@gmail.com


Public contact

Name of contact person

1st name
Middle name
Last name Lin yao tsung

Organization

Chi Mei Medical Center

Division name

anesthesiology department

Zip code


Address

No.901, Zhonghua Rd., Yongkang Dist., Tainan City 710, Taiwan (R.O.C.)

TEL

(06)281-2811-53321

Homepage URL


Email

anekevin@hotmail.com


Sponsor or person

Institute

Chi Mei Medical Center Medical Research Departmen

Institute

Department

Personal name



Funding Source

Organization

Chi Mei Medical Center Medical Research Department

Organization

Division

Category of Funding Organization

Outside Japan

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



Other administrative information

Date of disclosure of the study information

2016 Year 06 Month 12 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

Enrolling by invitation

Date of protocol fixation

2011 Year 09 Month 08 Day

Date of IRB


Anticipated trial start date

2012 Year 01 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

for identifying the risk factors, incidence and phenomenology of postoperative dleirium


Management information

Registered date

2016 Year 06 Month 12 Day

Last modified on

2016 Year 06 Month 12 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000026070


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name