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SPO2 VALIDATION STUDY - PHILIPS FAST 2025
NCT07221526 · View on ClinicalTrials.gov ↗
Study Summary
Clinical investigation is to validate the SpO2 accuracy of the M1133AX5, M1133AX6, and AlarX4 (nasal ala application) SpO2 sensors under test with the Philips FAST Pulse Oximetry technology.
Conditions Studied
Interventions
- DEVICE NO INTERVENTION
Study Locations (1)
Colorado
- Element Materials Technology — Louisville
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 72 participants |
| Start Date | 2025-10-28 |
| Est. Completion | 2026-01-09 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT07221526
The ClinicalTrials.gov registry entry for NCT07221526 describes a study currently listed as recruiting. It is categorized as an unspecified phase, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 72 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Philips Clinical & Medical Affairs Global, which has 186 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 1 condition, with PULSE OXIMETRY appearing as the primary indexed condition, and to 1 intervention — of which NO INTERVENTION is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT07221526 reports 1 study location spanning 1 distinct geographic area — top geographies include Colorado. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT07221526 about?
NCT07221526 is a clinical study titled "SPO2 VALIDATION STUDY - PHILIPS FAST 2025". Clinical investigation is to validate the SpO2 accuracy of the M1133AX5, M1133AX6, and AlarX4 (nasal ala application) SpO2 sensors under test with the Philips FAST Pulse Oximetry technology.
What is the current status of trial NCT07221526?
This trial is currently recruiting. The enrollment target is 72 participants. The study started on 2025-10-28. Estimated completion is 2026-01-09.
What conditions does trial NCT07221526 study?
This clinical trial studies the following conditions: PULSE OXIMETRY. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT07221526?
The interventions under investigation include: NO INTERVENTION (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT07221526?
This trial is sponsored by Philips Clinical & Medical Affairs Global, which has 186 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT07221526 being conducted?
This trial has 1 study location across Colorado. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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