Evaluating pulse oximeters during severe low oxygen levels
Accuracy of Pulse Oximeters With Profound Hypoxia
This study is testing how well a specific pulse oximeter works to measure oxygen levels in people who are experiencing very low oxygen levels.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 30 (estimated) |
| Ages | 18 Years to 55 Years |
| Sex | All |
| Sponsor | Consolidated Research, Inc. Industry-sponsored |
| Locations | 1 site (Cleveland, Ohio) |
| Trial ID | NCT06022523 on ClinicalTrials.gov |
What this trial studies
This clinical trial aims to collect photoplethysmography signals from pulse oximeters during episodes of profound hypoxia. The study follows established international standards to ensure accurate data acquisition. By analyzing the performance of the DT-400 pulse oximetry system under these conditions, the research seeks to improve the reliability of oxygen saturation measurements in critical situations.
Who should consider this trial
Good fit: Ideal candidates for this study are individuals experiencing episodes of profound hypoxia.
Not a fit: Patients who are pregnant will not benefit from this study due to exclusion criteria.
Why it matters
Potential benefit: If successful, this study could enhance the accuracy of pulse oximeters, leading to better patient outcomes in hypoxemic conditions.
How similar studies have performed: While there have been studies on pulse oximetry, this specific focus on profound hypoxia and adherence to international standards may present a novel approach.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: - Exclusion Criteria: Pregnancy -
Where this trial is running
Cleveland, Ohio
- Consolidated Research, Inc. — Cleveland, Ohio, United States (Recruiting)
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.