UMIN-CTR Clinical Trial
| Unique ID issued by UMIN | UMIN000024289 |
|---|---|
| Receipt number | R000026900 |
| Scientific Title | Association between telomere length and clinical indices in patients with idiopathic pulmonary fibrosis |
| Date of disclosure of the study information | 2016/10/07 |
| Last modified on | 2019/10/07 19:42:32 |
* This page includes information on clinical trials registered in UMIN clinical trial registed system.
* We don't aim to advertise certain products or treatments
Basic information
Public title
Association between telomere length and clinical indices in patients with idiopathic pulmonary fibrosis
Acronym
Telomere length in idiopathic pulmonary fibrosis
Scientific Title
Association between telomere length and clinical indices in patients with idiopathic pulmonary fibrosis
Scientific Title:Acronym
Telomere length in idiopathic pulmonary fibrosis
Region
| Japan |
Condition
Condition
Idiopathic pulmonary fibrosis (IPF)
Classification by specialty
| Pneumology |
Classification by malignancy
Others
Genomic information
YES
Objectives
Narrative objectives1
To investigate the natural course of the telomere length and determine whether the attrition of telomeres could be slowed by administration of antifibrotic agents in patients with idiopathic pulmonary fibrosis. Besides, we examine the relationship between telomere length and clinical indices.
Basic objectives2
Others
Basic objectives -Others
To explore whether the genetic mutation and allelic polymorphisms could associate with telomere length or clinical indices in patients with IPF.
Trial characteristics_1
Trial characteristics_2
Developmental phase
Not applicable
Assessment
Primary outcomes
Reduction in the telomere length attrition rate by administration of antifibrotic agent.
Key secondary outcomes
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
Patients diagnosed with idiopathic pulmonary fibrosis based on guidelines of an official ATS/ERS/JRS/ALAT statement.
Key exclusion criteria
(A)Retrospective study; patients who experienced the onset of malignant disease within 3 years from first visit for our hospital.
(B)Prospective study; (1) Patients with complication of malignant disease. But the patients who received complete resection or successful remission induction, and survived for more than 3 years without evidence of recurrence are eligible. (2) Patients who have been received more than 10mg/day of prednisolone or antifibrotic agents within 6 months. (3) Patients with acute exacerbation of IPF, respiratory infection, or pneumothorax within 4 weeks.
Target sample size
120
Research contact person
Name of lead principal investigator
| 1st name | Tomohiro |
| Middle name | |
| Last name | Handa |
Organization
Graduate School of Medicine, Kyoto University
Division name
Department of Respiratory Medicine
Zip code
606-8507
Address
54 Shougoin Kawahara-cho, Sakyo-ku, Kyoto, Japan
TEL
075-751-3830
hanta@kuhp.kyoto-u.ac.jp
Public contact
Name of contact person
| 1st name | Tomohiro |
| Middle name | |
| Last name | Handa |
Organization
Graduate School of Medicine, Kyoto University
Division name
Department of Respiratory Medicine
Zip code
606-8507
Address
54 Shogoin Kawahara-cho Sakyo-ku, Kyoto, Japan
TEL
075-751-3830
Homepage URL
hanta@kuhp.kyoto-u.ac.jp
Sponsor or person
Institute
Department of Respiratory Medicine, Graduate School of Medicine, Kyoto University
Institute
Department
Personal name
Funding Source
Organization
Japan Science and Technology Agency
Organization
Division
Category of Funding Organization
Japanese Governmental office
Nationality of Funding Organization
Other related organizations
Co-sponsor
Center for Genomic Medicine, Kyoto University. Department of Respiratory Medicine, Tenri Hospital. Department of Respiratory Medicine, Kobe City Medical Center General Hospital. Department of Respiratory Medicine, Kobe City Medical Center West Hospital. Department of Respiratory Medicine, Takatsuki Red Cross Hospital. Respiratory Disease Center, Tazuke Kofukai Medical Research Institute, Kitano Hospital. Department of Respiratory Medicine, National Hospital Organization Ibarakihigashi National Hospital. Department of Respiratory Medicine, Otsu Red Cross Hospital. Department of Respiratory Medicine, National Hospital Organization Himeji Medical Center. Department of Respiratory Medicine, Osaka Red Cross Hospital. Department of Respiratory Medicine, Kyoto City Hospital. Respiratory Disease Center, Rakuwakai Otowa Hospital. Department of Respiratory Medicine, Ohara HealthCare Foundation Kurashiki Central Hospital.
Name of secondary funder(s)
IRB Contact (For public release)
Organization
Ethics Committe, Kyoto University Hospital and Kyoto University Graduate School and Faculty of Medicine
Address
Konoe-cho Sakyo-ku, Kyoto, Japan
Tel
075-753-4680
ethcom@kuhp.kyoto-u.ac.jp
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
京都大学医学部附属病院（京都府）、公益財団法人天理よろづ相談所病院（奈良県）、神戸市立医療センター中央市民病院（兵庫県）、神戸市立医療センター西市民病院（兵庫県）、高槻赤十字病院（大阪府）、公益財団法人田附興風会医学研究所北野病院（大阪府）、独立行政法人国立病院機構茨城東病院（茨城県）、大津赤十字病院（滋賀県）、独立行政法人国立病院機構 姫路医療センター（兵庫県）、大阪赤十字病院（大阪府）、京都市立病院（京都府）、洛和会音羽病院（京都府）、公益財団法人大原記念倉敷中央医療機構 倉敷中央病院（岡山県）
Other administrative information
Date of disclosure of the study information
| 2016 | Year | 10 | Month | 07 | 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
| 2016 | Year | 08 | Month | 20 | Day |
Date of IRB
| 2016 | Year | 11 | Month | 24 | Day |
Anticipated trial start date
| 2016 | Year | 11 | Month | 24 | Day |
Last follow-up date
| 2021 | Year | 05 | Month | 23 | Day |
Date of closure to data entry
Date trial data considered complete
Date analysis concluded
Other
Other related information
This study is composed of retrospective and prospective study;
(A) Retrospective study, for example, is time-series analysis or descriptive epidemiology.(B) Prospective study is cohort that conducts a longitudinal assessment of patients with IPF.
Management information
Registered date
| 2016 | Year | 10 | Month | 04 | Day |
Last modified on
| 2019 | Year | 10 | Month | 07 | Day |
Link to view the page
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000026900
| Research Plan | |
|---|---|
| Registered date | File name |
| Research case data specifications | |
|---|---|
| Registered date | File name |
| Research case data | |
|---|---|
| Registered date | File name |
