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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register.
Register: JPRN
Last refreshed on: 17 October 2023
Main ID:  JPRN-UMIN000008541
Date of registration: 30/07/2012
Prospective Registration: Yes
Primary sponsor: Department of Respiratory Medicine and Allergology, Kinki University Faculty of Medicine
Public title: The effect of pirfenidone on the mortality risk score in IPF
Scientific title: The effect of pirfenidone on the mortality risk score in IPF - The effect of pirfenidone on the mortality risk score in IPF
Date of first enrolment: 2012/07/30
Target sample size: 20
Recruitment status: Complete: follow-up complete
URL:  https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000010041
Study type:  Interventional
Study design:  Single arm Non-randomized  
Phase:  Not applicable
Countries of recruitment
Japan
Contacts
Name:     Osamu Nishiyama, MD
Address:  377-2 Onohigashi, Osaka-sayama, Osaka 589-8511, Japan Japan
Telephone: 072-366-0221
Email: nishi-o@med.kindai.ac.jp
Affiliation:  Kinki University Faculty of Medicine Department of Respiratory Medicine and Allergology
Name:     Osamu Nishiyama, MD
Address:  377-2 Onohigashi, Osaka-sayama, Osaka 589-8511, Japan Japan
Telephone: 072-366-0221
Email: nishi-o@med.kindai.ac.jp
Affiliation:  Kinki University Faculty of Medicine Department of Respiratory Medicine and Allergology
Key inclusion & exclusion criteria
Inclusion criteria:
Exclusion criteria: 1. Diagnosis of malignancies 2. Unable to undergo pulmonary function test and 6-min walk test 3. Already taking pirfenidone 4. A history of severe toxicity of pirfenidone 5. Undergoing long-term oxygen therapy at rest

Age minimum: 20years-old
Age maximum: Not applicable
Gender: Male and Female
Health Condition(s) or Problem(s) studied
idiopathic pulmonary fibrosis
Intervention(s)
pirfenidone
Primary Outcome(s)
mortality risk score
Secondary Outcome(s)
1. pulmonary function test 2. 6-min walk test 3. dyspnea 4. chest HRCT findings
Secondary ID(s)
Source(s) of Monetary Support
none
Secondary Sponsor(s)
Ethics review
Status: YES
Approval date:
Contact:
Results
Results available: Yes
Date Posted:
Date Completed: 18/12/2014
URL:
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