UMIN-CTR Clinical Trial
| Unique ID issued by UMIN | UMIN000002764 |
|---|---|
| Receipt number | R000003358 |
| Scientific Title | Bronchodilator effects of salmeterol/fluticasone propionate (SFC) in patients with COPD |
| Date of disclosure of the study information | 2009/11/13 |
| Last modified on | 2013/04/11 16:26:49 |
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Basic information
Public title
Bronchodilator effects of salmeterol/fluticasone propionate (SFC) in patients with COPD
Acronym
Bronchodilator effects of salmeterol/fluticasone propionate (SFC) in patients with COPD
Scientific Title
Bronchodilator effects of salmeterol/fluticasone propionate (SFC) in patients with COPD
Scientific Title:Acronym
Bronchodilator effects of salmeterol/fluticasone propionate (SFC) in patients with COPD
Region
| Japan |
Condition
Condition
COPD
Classification by specialty
| Pneumology |
Classification by malignancy
Others
Genomic information
NO
Objectives
Narrative objectives1
To examine clinical effects of SFC in patients with COPD by using pulmonary function, induced sputum, chest computed tomography, health-related quality of life.
Basic objectives2
Efficacy
Basic objectives -Others
Trial characteristics_1
Confirmatory
Trial characteristics_2
Developmental phase
Assessment
Primary outcomes
Indices of chest CT
Key secondary outcomes
Parameters of pulmonary function
Cell counts of induced sputum
Scores of quality of life
Base
Study type
Interventional
Study design
Basic design
Single arm
Randomization
Non-randomized
Randomization unit
Blinding
Open -but assessor(s) are blinded
Control
No treatment
Stratification
Dynamic allocation
Institution consideration
Blocking
Concealment
Intervention
No. of arms
1
Purpose of intervention
Treatment
Type of intervention
| Medicine |
Interventions/Control_1
Inhaled SFC (50/250) twice daily.
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
COPD patients meet the GOLD guidelines (post-bronchodilator FEV1/forced vital capacity (FVC) ratio < 70%).
Key exclusion criteria
1) Asthma
2) Subjects had taken corticosteroids (either oral or inhaled)
3) Subjects had been suffering from COPD exacerbation.
4) Patients who are considered inappropriate by doctor.
Target sample size
30
Research contact person
Name of lead principal investigator
| 1st name | |
| Middle name | |
| Last name | Makoto Hoshino |
Organization
Atami Hospital
International University of Health and Welfare
Division name
Department of Respiratory Medicine
Zip code
Address
13-1 Higashikaigan-cho, Atami
TEL
0557819171
Public contact
Name of contact person
| 1st name | |
| Middle name | |
| Last name | Makoto Hoshino |
Organization
Atami Hospita International University of Health and Welfare
Division name
Department of Respiratory Medicine
Zip code
Address
13-1 Higashikaigan-cho, Atami
TEL
0557819171
Homepage URL
hoshino@iuhw.ac.jp
Sponsor or person
Institute
Atami Hospita International
University of Health and Welfare
Institute
Department
Personal name
Funding Source
Organization
none
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
| 2009 | Year | 11 | Month | 13 | 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
Completed
Date of protocol fixation
| 2009 | Year | 07 | Month | 20 | Day |
Date of IRB
Anticipated trial start date
| 2009 | Year | 10 | Month | 01 | Day |
Last follow-up date
| 2012 | Year | 12 | Month | 01 | Day |
Date of closure to data entry
Date trial data considered complete
Date analysis concluded
Other
Other related information
Management information
Registered date
| 2009 | Year | 11 | Month | 13 | Day |
Last modified on
| 2013 | Year | 04 | Month | 11 | Day |
Link to view the page
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000003358
