FDA-Approved device monitored for Long-Term dialysis safety
NCT ID NCT07146854
Summary
This study is collecting long-term safety and performance information on an already FDA-approved device called EndoForce. The device is used to connect a dialysis graft to a vein in patients with end-stage kidney disease. Researchers will follow 150 patients to see how well the connection holds up and track any related health issues over time.
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Contacts and locations
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Study contacts
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Contact
Phone: •••-•••-•••• Email: •••••@•••••
Locations
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MUSC Health Orangeburg
NOT_YET_RECRUITINGOrangeburg, South Carolina, 29118, United States
Contact
Contact Phone: •••-•••-•••• Email: •••••@•••••
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Spartanburg Regional Medical Center
RECRUITINGSpartanburg, South Carolina, 29303, United States
Contact
Contact Phone: •••-•••-•••• Email: •••••@•••••
Conditions
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