UMIN-CTR Clinical Trial
| Unique ID issued by UMIN | UMIN000021707 |
|---|---|
| Receipt number | R000025043 |
| Scientific Title | Clinical significance and reproducibitity of measurement of health status using COPD assessment test (CAT) in elderly patients with COPD |
| Date of disclosure of the study information | 2016/03/31 |
| Last modified on | 2016/04/05 10:20:35 |
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Basic information
Public title
Clinical significance and reproducibitity of measurement of health status using COPD assessment test (CAT) in elderly patients with COPD
Acronym
Clinical significance of measurement of health status using COPD assessment test (CAT) in elderly patients with COPD
Scientific Title
Clinical significance and reproducibitity of measurement of health status using COPD assessment test (CAT) in elderly patients with COPD
Scientific Title:Acronym
Clinical significance of measurement of health status using COPD assessment test (CAT) in elderly patients with COPD
Region
| Japan |
Condition
Condition
COPD
Classification by specialty
| Pneumology |
Classification by malignancy
Others
Genomic information
NO
Objectives
Narrative objectives1
The first aim of the present study is to examine the reproducibility of COPD assessment test (CAT) measurement in the elderly patients with COPD. Secondly, we examined the efficacy of the CAT in evaluating the health-related quality of life (HRQOL) of elderly patients with COPD treated with bronchodilators.clinical significance of CAT assessement in elderly COPD patients
Basic objectives2
Others
Basic objectives -Others
Trial characteristics_1
Others
Trial characteristics_2
Others
Developmental phase
Not applicable
Assessment
Primary outcomes
The reproducibility of COPD assessment test (CAT) measurement in the elderly patients with COPD
Key secondary outcomes
The resposne to bronchodilator treatment in elderly COPD patients
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
| 40 | years-old | <= |
Age-upper limit
| 90 | years-old | > |
Gender
Male and Female
Key inclusion criteria
Clinically stable patients with moderate to severe COPD,who are 40 years of age or older and have smoking history or current smokers and stop smoking at the time of giving the consent to this study..
They all provide written, informed consent
Key exclusion criteria
Exclusion criteria: (1) Coexistence of other major pulmonary diseases such as asthma, bronchiectasis, pulmonary fibrosis, tuberculosis, and pulmonary cancer diagnosed by imaging modalities and/or laboratory findings. Asthma is excluded based on clinical history and/or laboratory findings, including levels of IgE and/or eosinophils in blood and/or sputum, but not based on reversibility of airflow limitation.
(2)patients with cancers
(3)patients with other serious complocations
(4) Those who are considered as inappropriate subjects for any reasons.
Target sample size
100
Research contact person
Name of lead principal investigator
| 1st name | |
| Middle name | |
| Last name | Shinji Teramoto |
Organization
Hitachinaka General Hospital
Division name
Department of pulmonary medicine
Zip code
Address
20-1 Ishikawa-cho, Hitachinaka-shi, Ibaraki,Japan 312-0057
TEL
029-354-5111
shinjit-tky@umin.ac.jp
Public contact
Name of contact person
| 1st name | |
| Middle name | |
| Last name | Shinji Teramoto |
Organization
Hitachinaka General Hospital
Division name
Department of pulmonary medicine
Zip code
Address
20-1 Ishikawa-cho Hitachinaka-shi
TEL
029-354-5111
Homepage URL
shinjit-tky@umin.ac.jp
Sponsor or person
Institute
Hitachinaka General Hospital
Institute
Department
Personal name
Funding Source
Organization
Hitachinaka General 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
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 | 03 | Month | 31 | 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
| 2012 | Year | 03 | Month | 29 | Day |
Date of IRB
Anticipated trial start date
| 2013 | Year | 04 | Month | 01 | Day |
Last follow-up date
| 2017 | Year | 04 | Month | 01 | Day |
Date of closure to data entry
| 2017 | Year | 04 | Month | 01 | Day |
Date trial data considered complete
| 2017 | Year | 04 | Month | 01 | Day |
Date analysis concluded
| 2017 | Year | 08 | Month | 01 | Day |
Other
Other related information
The results will be presented in the Journals
Management information
Registered date
| 2016 | Year | 03 | Month | 31 | Day |
Last modified on
| 2016 | Year | 04 | Month | 05 | Day |
Link to view the page
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000025043
