Observation of Wheeled Device Use After TKA (NCT06080152)

🧪 Interventions in This Study

• Mobility Tool (DEVICE)

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

📍 All Participating Trial Locations (1 Sites)

• 450 Broadway — Redwood City, California

📞 Contact the Study Coordinator

Phone: (650) 723-2257

Email: DFA@stanford.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 Total Knee Arthroplasty

• Safety and Performance Study of the Legion Porous System in Total Knee Arthroplasty — Coon Rapids, Minnesota
• NitrX Total Knee Arthroplasty RSA — London, Ontario
• Bicruciate-retaining (2C) Total Knee Arthroplasty (TKA) Versus Posterior-stabilized (PS) Total Knee Arthroplasty (TKA) — Montreal, Quebec
• Safety and Performance Using Legion™ CR Oxinium and CoCr Femoral Implants Combined With Legion™/Genesis™ II XLPE High Flex Tibial Inserts — Edina, Minnesota
• Incidence of Adductor Canal Catheter Dislodgment — Toronto, Ontario
• IO Vancomycin Administration in TKA — San Diego, California

Explore by condition: All Total Knee Arthroplasty 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.