Hypoxia and Hemodilution Testing in Healthy Adult Volunteers (NCT07503171)

🧪 Interventions in This Study

• Noninvasive Physiological Monitoring Device (DEVICE)

Full eligibility criteria are available on the official NIH protocol. View the criteria ↗

📍 All Participating Trial Locations (1 Sites)

• Vital Sign Research Group — San Francisco, California

📞 Contact the Study Coordinator

Phone: (650) 868-5155

Email: stratman@anesthesia.ucsf.edu

Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.

💰 Cost, Insurance & Patient Rights

• 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
• Routine Patient Care: Under federal law (ACA § 2709) and many state statutes, routine care costs are covered during participation.
• Voluntary Participation: You may withdraw at any time without affecting your standard medical care.

More studies in Hypoxia

• Pulse Oximeter Accuracy During Stable Hypoxia Plateaus — San Francisco, California
• Determination of SpO2 and PR Accuracy Specifications at Rest (71Ag_Vital-0031) — San Francisco, California
• Graded Exercise Hypoxia Testing — Rochester, Minnesota
• Intravenous Iron Effects on Performance at High Altitude — Natick, Massachusetts
• Pulse Oximeter Accuracy in Healthy Humans During Hypoxia — San Francisco, California

Explore by condition: All Hypoxia clinical trials

💡 How to Participate

1. Check the checklist above to see if you may qualify.
2. Contact the study coordinator using the phone/email above.
3. Ask about the visit schedule, what is covered at no cost, and any travel support.
4. Confirm with your own doctor before making a decision.