UMIN-CTR Clinical Trial

Basic information
Official scientific title of the study	Identifying postoperative delirium by a quick, systemic method-" the nursing delirium screening scale"
Title of the study (Brief title)	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

In outcomes field, the entry of just a few words such as "safety" or "efficiency" will not be accepted. Specify the name of outcome measures, including the time when you plan to measure. Usually, only one primary outcome is accepted. Write the other outcomes in "secondary outcomes" field.

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

In interventions field, include the details of interventions, such as duration, amount, and frequency. If the intervention includes prescription or use of medical devices, duration is required.

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	Chen jenyin
Organization	Chi Mei Medical Center
Division name	anesthesiology department
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	Lin yao tsung
Organization	Chi Mei Medical Center
Division name	anesthesiology department
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
Institute	Chi Mei Medical Center Medical Research Departmen
Institute
Department

Sponsor means an organization that is responsible for plan, deployment and report of the research including funding management. It doesn't mean funding agency". Therefore, all clinical trial should have the one.

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)

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

Progress
Recruitment status	Enrolling by invitation
Date of protocol fixation	2011 Year 09 Month 08 Day
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

Related information
URL releasing protocol
Publication of results	Unpublished
URL releasing results
Results
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
URL(English)	https://upload.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000026070