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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-UMIN000005098
Date of registration: 18/02/2011
Prospective Registration: No
Primary sponsor: Department of Respiratory Medicine and Allergology, Kinki University School of Medicine
Public title: A randomized trial of ambulatory oxygen in patients with idiopathic pulmonary fibrosis and desaturation but without resting hypoxemia
Scientific title: A randomized trial of ambulatory oxygen in patients with idiopathic pulmonary fibrosis and desaturation but without resting hypoxemia - ambulatory oxygen in patients with IPF and desaturation but without resting hypoxemia
Date of first enrolment: 2011/02/01
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=R000006057
Study type:  Interventional
Study design:  Cross-over Randomized  
Phase:  Not selected
Countries of recruitment
Japan
Contacts
Name:     Osamu Nishiyama
Address:  377-2 Onohigashi, Osaka-sayama, Osaka, Japan Japan
Telephone: 072-366-0221
Email: nishi-o@med.kindai.ac.jp
Affiliation:  Kinki University School of Medicine Department of Respiratory Medicine and Allergology
Name:     Osamu Nishiyama
Address:  377-2 Onohigashi, Osaka-sayama, Osaka, Japan Japan
Telephone: 072-366-0221
Email: nishi-o@med.kindai.ac.jp
Affiliation:  Kinki University School of Medicine Department of Respiratory Medicine and Allergology
Key inclusion & exclusion criteria
Inclusion criteria:
Exclusion criteria: 1) patients with uncontrolled comorbidities 2) patients who cannot undergo pulmonary function test and/or 6-min walk test

Age minimum: 20years-old
Age maximum: Not applicable
Gender: Male and Female
Health Condition(s) or Problem(s) studied
idiopathic pulmonary fibrosis
Intervention(s)
ambulatory oxygen
ambulatory air
Primary Outcome(s)
dyspnea after 6-min walk
Secondary Outcome(s)
O2 saturation after 6-min walk 6-min walk distance fatigue after 6-min walk heart rate after 6-min walk
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: 01/05/2012
URL: http://www.ncbi.nlm.nih.gov/pubmed/23806287
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