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This first-in-human pilot study seeks to evaluate the feasibility and safety of using a percutaneous ultrasound device with needle guide for vascular access. Eligible participants will undergo the pro...
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Lead Sponsor
Johns Hopkins University
Collaborators
NCT07509359 · Vascular Access Device Complications
NCT06001827 · Chronic Kidney Diseases, End Stage Renal Disease, and more
NCT07179536 · Femoral Access Site Closure, Ambulation, and more
NCT06770374 · Vascular Access Complication, Skin and Subcutaneous Tissue Disorders, and more
NCT05490238 · Vascular Access Site Occlusion
Johns Hopkins School of Medicine
Baltimore, Maryland
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This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
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