UMIN-CTR Clinical Trial
| Unique ID issued by UMIN | UMIN000018094 |
|---|---|
| Receipt number | R000020943 |
| Scientific Title | Safety and efficacy of bioabsorbable stent in percutaneous transluminal pulmonary angioplasty |
| Date of disclosure of the study information | 2015/07/01 |
| Last modified on | 2015/06/25 22:15:14 |
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Basic information
Public title
Safety and efficacy of bioabsorbable stent in percutaneous transluminal pulmonary angioplasty
Acronym
Safety and efficacy of bioabsorbable stent in percutaneous transluminal pulmonary angioplasty
Scientific Title
Safety and efficacy of bioabsorbable stent in percutaneous transluminal pulmonary angioplasty
Scientific Title:Acronym
Safety and efficacy of bioabsorbable stent in percutaneous transluminal pulmonary angioplasty
Region
| Japan |
Condition
Condition
pulmonary embolism(including chronic thromboembolic pulmonary hypertension) and pulmonary stenosis
Classification by specialty
| Cardiology |
Classification by malignancy
Others
Genomic information
NO
Objectives
Narrative objectives1
To evaluate the safety and efficacy of bioabsorbable stent placed into pulmonary arteries
Basic objectives2
Safety,Efficacy
Basic objectives -Others
Trial characteristics_1
Trial characteristics_2
Developmental phase
Assessment
Primary outcomes
Evaluation of the conditions of placed bioabsorbable stent and treated pulmonary arteries, such as restenosis
Key secondary outcomes
Base
Study type
Study design
Basic design
Parallel
Randomization
Non-randomized
Randomization unit
Blinding
Open -no one is blinded
Control
No treatment
Stratification
Dynamic allocation
Institution consideration
Blocking
Concealment
Intervention
No. of arms
2
Purpose of intervention
Treatment
Type of intervention
| Device,equipment |
Interventions/Control_1
Placement of bioabsorbable stent into pulmonary artery in percutaneous transluminal pulmonary angioplasty
Interventions/Control_2
Balloon dilation in percutaneous transluminal pulmonary angioplasty
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
age > 20 years old
patients whose informed consents can be taken by their own wills
Key exclusion criteria
bad compliance regarding medicines such as anti-coagulation drugs
Target sample size
20
Research contact person
Name of lead principal investigator
| 1st name | |
| Middle name | |
| Last name | Keiichi Fukuda |
Organization
Keio University School of Medicine
Division name
Department of Cardiology
Zip code
Address
Shinanomachi 35, Shinjuku-ku, Tokyo, Japan
TEL
03-3353-1211
kfukuda@a2.keio.jp
Public contact
Name of contact person
| 1st name | |
| Middle name | |
| Last name | Takashi Kawakami |
Organization
Keio University School of Medicine
Division name
Department of Cardiology
Zip code
Address
Shinanomachi 35, Shinjuku-ku, Tokyo, Japan
TEL
03-3353-1211
Homepage URL
kawakami.1650@gmail.com
Sponsor or person
Institute
Keio University School of Medicine
Institute
Department
Personal name
Funding Source
Organization
Research funding of research contact person
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
| 2015 | Year | 07 | Month | 01 | 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
Open public recruiting
Date of protocol fixation
| 2014 | Year | 11 | Month | 28 | Day |
Date of IRB
Anticipated trial start date
| 2015 | Year | 07 | Month | 01 | Day |
Last follow-up date
Date of closure to data entry
Date trial data considered complete
Date analysis concluded
Other
Other related information
Management information
Registered date
| 2015 | Year | 06 | Month | 25 | Day |
Last modified on
| 2015 | Year | 06 | Month | 25 | Day |
Link to view the page
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000020943
