Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT01961362 · ClinicalTrials.gov registry record

Supplemental Oxygen in Pulmonary Fibrosis

A clinical trial, sponsored by National Jewish Health.

Completed
Registry status
19
Enrollment target

NCT01961362: Completed study, sponsored by National Jewish Health.

NCT01961362 is a clinical trial that has completed, run by National Jewish Health. The registered enrollment target is 19 participants. According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT01961362 has completed, sponsored by National Jewish Health.

COMPLETED
Registry status
19 participants
Enrollment target

Study Summary

To enhance understanding of supplemental oxygen-its utility in and adoption by patients with pulmonary fibrosis-by examining how patients perceive it and by determining how perceptions and patient-centered outcome measures change from before to after supplemental oxygen is prescribed.

Primary Outcome

The University of California San Diego Shortness of Breath Questionnaire (or UCSD SOB) is a tool that measures shortness of breath using 24 items, each with response options ranging from 0 to 5, corresponding to "None at all" and "Maximally or unable to do because of breathlessness." Thus, scores for the UCSD SOB range from 0 to 120, with higher scores indicating greater shortness of breath.

Trial Details

FieldValue
Enrollment Target 19 participants
Start Date 2013-10
Est. Completion 2016-12
National Jewish Health

83 total trials

What the finished NCT01961362 record still lists

NCT01961362 is an observational study that tracks outcomes without assigning an intervention. The registry caps enrollment at 19 participants, a relatively small participant target.

The record links to 0 conditions, and to 0 interventions.

NCT01961362 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01961362 about?

NCT01961362 is a clinical study titled "Supplemental Oxygen in Pulmonary Fibrosis". To enhance understanding of supplemental oxygen-its utility in and adoption by patients with pulmonary fibrosis-by examining how patients perceive it and by determining how perceptions and patient-centered outcome measures change from before to after supplemental oxygen is prescribed.

What is the current status of trial NCT01961362?

This trial is currently completed. The enrollment target is 19 participants. The study started on 2013-10. Estimated completion is 2016-12.

Who is sponsoring clinical trial NCT01961362?

This trial is sponsored by National Jewish Health, which has 83 total clinical trials registered on ClinicalTrials.gov.

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT03207464 · 19 participants · Phase 1

    Molecular Imaging of NET Using [C-11]MRB-PET in MS

  • NCT04318717 · 19 participants · Phase 2

    Pembrolizumab and Hypofractionated Radiation Therapy for the Treatment of Mucosal Melanoma

  • NCT05103904 · 19 participants · Phase 2

    Lenvatinib for the Treatment of Recurrent Hepatocellular Carcinoma After Liver Transplant

  • NCT05607407 · 19 participants · Phase 2

    Methimazole in Patients With Progressive Glioblastoma

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT01961362, the US trial registry maintained by the National Library of Medicine. NCT01961362 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.