UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000016179
Receipt number R000018782
Scientific Title The prospective observational study to evaluate swallowing ability in patients with Nursing and Healthcare Associated Pneumonia (NHCAP) categorized as group B or C or D according to the JRS Guidelines for the Management of Nursing and Healthcare Associated pneumonia in Adults
Date of disclosure of the study information 2015/01/11
Last modified on 2018/01/13 14:16:25

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Basic information

Public title

The prospective observational study to evaluate swallowing ability in patients with Nursing and Healthcare Associated Pneumonia (NHCAP) categorized as group B or C or D according to the JRS Guidelines for the Management of Nursing and Healthcare Associated pneumonia in Adults

Acronym

The prospective observational study to evaluate swallowing ability in patients with NHCAP group B/C/D according to the JRS Guidelines

Scientific Title

The prospective observational study to evaluate swallowing ability in patients with Nursing and Healthcare Associated Pneumonia (NHCAP) categorized as group B or C or D according to the JRS Guidelines for the Management of Nursing and Healthcare Associated pneumonia in Adults

Scientific Title:Acronym

The prospective observational study to evaluate swallowing ability in patients with NHCAP group B/C/D according to the JRS Guidelines

Region

Japan


Condition

Condition

Nursing and Healthcare Associated Pneumonia

Classification by specialty

Pneumology Infectious disease

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To evaluate prospectively swallowing ability in patients with NHCAP categorized as group B or C or D according to the JRS Guidelines for the Management of Nursing and Healthcare Associated Pneumonia in Adults

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

30-day mortality

Key secondary outcomes

Relapses of pneumonia occurring within 30 days following admission


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

1. Patients 20 years of age and older
2. Patients with NHCAP categorized as group B or C or D according to the JRS Guidelines for the Management of Nursing and Healthcare Associated Pneumonia in Adults

Key exclusion criteria

Patients deemed ineligible by the attending physicians for various reasons

Target sample size

100


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Tatuji Katou

Organization

Tobata Kyoritsu Hospital

Division name

Department of Respiratory Medicine

Zip code


Address

2-5-1 Sawami, Tobata-ku, Kitakyushu city, Fukuoka, 804-0093, Japan

TEL

093-871-5421

Email

t-katou@kyoaikai.com


Public contact

Name of contact person

1st name
Middle name
Last name Yasuo Chojin

Organization

Tobata Kyoritsu Hospital

Division name

Department of Respiratory Medicine

Zip code


Address

2-5-1 Sawami, Tobata-ku, Kitakyushu city, Fukuoka, 804-0093, Japan

TEL

093-871-5421

Homepage URL


Email

choppy001042@yahoo.co.jp


Sponsor or person

Institute

Department of Respiratory Medicine, Tobata Kyoritsu Hospital

Institute

Department

Personal name



Funding Source

Organization

Department of Respiratory Medicine, Tobata Kyoritsu Hospital

Organization

Division

Category of Funding Organization

Self funding

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

2015 Year 01 Month 11 Day


Related information

URL releasing protocol


Publication of results

Published


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

Main results already published

Date of protocol fixation

2015 Year 01 Month 13 Day

Date of IRB


Anticipated trial start date

2015 Year 01 Month 13 Day

Last follow-up date


Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information

This study is prospective observation study. Patients with NHCAP in attending hospital are enrolled.


Management information

Registered date

2015 Year 01 Month 11 Day

Last modified on

2018 Year 01 Month 13 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000018782


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name