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A Prospective Observational Study of the Breath Responsive Variable Bolus Oxygen Conserving Device

NCT02627599 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 35

Last updated 2018-08-15

No results posted yet for this study

Summary

* Evaluate subjects in an prospective observational study
* Subjects will be administered scientifically validated questionnaires
* Evaluate Quality Improvement and Oxygen Utilization Improvements.

1\. Functional capability, dyspnea, oxygen saturation as primary endpoints
1. Baseline Dyspnea Index (BDI)
2. Transitional Dyspnea Index (TDI)
3. Chronic Respiratory Disease Questionnaire (CRQ)
4. Six minute walk distance (6MWD)
5. Oxygen saturation using pulse oximeter
* The secondary endpoints:

1. Portable oxygen source utilization
2. Health care utilization (emergency room encounters, hospital admissions)

Conditions

Interventions

DEVICE

Breath Responsive Variable Bolus Oxygen Conserving Device

Mini Electronic Oxygen Conserving Device

Sponsors & Collaborators

Principal Investigators

  • Isabel Pereira, MD · StratiHealth

Eligibility

Min Age
65 Years
Max Age
85 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2015-05-31
Primary Completion
2016-11-30
Completion
2016-11-30

Countries

  • United States

Study Locations

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Entities

Diseases
Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02627599 on ClinicalTrials.gov