Validation and Feasibility of Noninvasive Oxygen Delivery Index Monitoring in Cardiac Surgery Patients (NCT07573306)

🧪 Interventions in This Study

• SpHb monitor (DEVICE)

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

📍 All Participating Trial Locations (1 Sites)

• University of Minnesota — Minneapolis, Minnesota

📞 Contact the Study Coordinator

Phone: (612) 282-3705

Email: landr184@umn.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 Cardiac Surgery

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• Ketamine and Kidney Injury in Cardiac Surgery — Rochester, Minnesota
• Prevalence and Clinical Impact of Airway Opening Pressure in Post-Cardiac Surgery Patients — Québec, Quebec
• A Randomized Clinical Trial to Measure Efficacy of Music on Cardiac Surgery Patients — Boston, Massachusetts
• Low Tidal Volume Ventilation With Hyperoxia Avoidance During Cardiopulmonary Bypass (The FOCUS Trial) — Cleveland, Ohio
• Randomized Evaluation of Operating Room Extubation After Cardiac Surgery — Boston, Massachusetts

Explore by condition: All Cardiac Surgery 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.