UMIN-CTR Clinical Trial
| Unique ID issued by UMIN | UMIN000003105 |
|---|---|
| Receipt number | R000003766 |
| Scientific Title | Clinical efficasy of Montelukast-early-intervention for Japanese cedar pollinosis |
| Date of disclosure of the study information | 2010/01/27 |
| Last modified on | 2011/02/22 06:06:53 |
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Basic information
Public title
Clinical efficasy of Montelukast-early-intervention for Japanese cedar pollinosis
Acronym
Clinical efficasy of Montelukast for Japanese cedar pollinosis
Scientific Title
Clinical efficasy of Montelukast-early-intervention for Japanese cedar pollinosis
Scientific Title:Acronym
Clinical efficasy of Montelukast for Japanese cedar pollinosis
Region
| Japan |
Condition
Condition
Japanese cedar pollinosis
Classification by specialty
| Oto-rhino-laryngology |
Classification by malignancy
Others
Genomic information
NO
Objectives
Narrative objectives1
We examimned the efficacy of montelukas-early-intervention for Japanese cedar pollinosis and also looked at the effect of combined therapy using, a randomized, double-blined, placebo-controlled study during pollen-season.
Basic objectives2
Efficacy
Basic objectives -Others
Trial characteristics_1
Confirmatory
Trial characteristics_2
Explanatory
Developmental phase
Phase IV
Assessment
Primary outcomes
Effect of leukotriene antagonist
Key secondary outcomes
Nitric oxiside consentration in airway
Base
Study type
Interventional
Study design
Basic design
Cross-over
Randomization
Randomized
Randomization unit
Individual
Blinding
Double blind -all involved are blinded
Control
Placebo
Stratification
NO
Dynamic allocation
NO
Institution consideration
Institution is considered as a block.
Blocking
NO
Concealment
Central registration
Intervention
No. of arms
3
Purpose of intervention
Treatment
Type of intervention
| Medicine |
Interventions/Control_1
It is given montelukast 10mg, 1 capsule per 1 day, from a week before until the end of Japanese pollen season.
Interventions/Control_2
It is given montelukast 10mg, 1 capsule per 1 day, from a week before until the end of Japanese pollen season, also and given loratadine 10 mg per 1 day, from peak-season until the end of Japanese pollen season.
Interventions/Control_3
It is given montelukast 10mg, 1 capsule per 1 day, from a week before until the end of Japanese pollen season, also and given a placebo capsule per 1 day, from peak-season until the end of Japanese pollen season.
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
| 18 | years-old | <= |
Age-upper limit
| 60 | years-old | >= |
Gender
Male and Female
Key inclusion criteria
Being over class 2 in CAP-RAST against Japanese Cedar pollen over, and having clinicalsymptoms during Japanese cedar pollen season.
Key exclusion criteria
Pregnancy, potential pregnancy, and breas-feeding patient.
Target sample size
150
Research contact person
Name of lead principal investigator
| 1st name | |
| Middle name | |
| Last name | Shigeharu Fujieda |
Organization
Faculty of Medicine, University of Fukui
Division name
Ororhinolaryngology, Head and Neck Surgery
Zip code
Address
23 Matsuoka-Shimoaizuki, Eiheiji, Yoshida, Fukui, Japan
TEL
0776-61-8407
Public contact
Name of contact person
| 1st name | |
| Middle name | |
| Last name | Takechiyo Yamada |
Organization
Faculty of Medicine, University of Fukui
Division name
Ororhinolaryngology, Head and Neck Surgery
Zip code
Address
23 Matsuoka-Shimoaizuki, Eiheiji, Yoshida, Fukui, Japan
TEL
0776-61-8407
Homepage URL
Sponsor or person
Institute
Faculty of Medicine, University of Fukui
Institute
Department
Personal name
Funding Source
Organization
Ororhinolaryngology, Head and Neck Surgery, Faculty of Medicine, University of Fukui
Organization
Division
Category of Funding Organization
Self funding
Nationality of Funding Organization
Japan
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
| 2010 | Year | 01 | Month | 27 | Day |
Related information
URL releasing protocol
Publication of results
Partially 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
Completed
Date of protocol fixation
| 2009 | Year | 12 | Month | 01 | Day |
Date of IRB
Anticipated trial start date
| 2010 | Year | 01 | Month | 01 | Day |
Last follow-up date
| 2010 | Year | 04 | Month | 01 | Day |
Date of closure to data entry
| 2010 | Year | 05 | Month | 01 | Day |
Date trial data considered complete
| 2010 | Year | 10 | Month | 01 | Day |
Date analysis concluded
| 2010 | Year | 12 | Month | 01 | Day |
Other
Other related information
Management information
Registered date
| 2010 | Year | 01 | Month | 27 | Day |
Last modified on
| 2011 | Year | 02 | Month | 22 | Day |
Link to view the page
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000003766
