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NCT02814721 · ClinicalTrials.gov registry record · NA
Coronal Mode Ultrasound Guided Hemodialysis Cannulation: Comparison With Standard Cannulation Technique
A NA study, sponsored by Henry Ford Health System.
- Completed
- Registry status
- NA
- Development phase
- 10
- Enrollment target
NCT02814721 is a NA study that has completed, run by Henry Ford Health System. The registered enrollment target is 10 participants.
The verdict
NCT02814721, a NA study, has completed, sponsored by Henry Ford Health System.
- COMPLETED
- Registry status
- NA
- Development phase
- 10 participants
- Enrollment target
Study Summary
Infiltrations from cannulation difficulties result in significant morbidity including loss of vascular access (VA) loss in hemodialysis (HD). Cannulation is reliant on personnel skill and VA characteristics. Surface marking of VA lacks real-time information and traditional ultrasound (US) devices are large, expensive and require skilled operator expertise. Sonic Window© (Analogic Ultrasound, Peabody, MA) is a coronal mode ultrasound device (CMUD) approved for VA cannulation. Study is a single center randomized, prospective pilot study comparing handheld US-guided cannulation of new arteriovenous fistula (AVF) to standard cannulation practices.
Interventions
- DEVICE Sonic Window ultrasound device
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 10 participants |
| Start Date | 2015-03 |
| Est. Completion | 2015-12 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT02814721
The ClinicalTrials.gov registry entry for NCT02814721 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 10 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Henry Ford Health System, which has 234 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 1 intervention - of which Sonic Window ultrasound device is the first listed.
NCT02814721 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT02814721 about?
NCT02814721 is a clinical study titled "Coronal Mode Ultrasound Guided Hemodialysis Cannulation: Comparison With Standard Cannulation Technique". Infiltrations from cannulation difficulties result in significant morbidity including loss of vascular access (VA) loss in hemodialysis (HD). Cannulation is reliant on personnel skill and VA characteristics. Surface marking of VA lacks real-time information and traditional ultrasound (US) devices ar...
What is the current status of trial NCT02814721?
This trial is currently completed. It is a NA study. The enrollment target is 10 participants. The study started on 2015-03. Estimated completion is 2015-12.
What interventions are being tested in trial NCT02814721?
The interventions under investigation include: Sonic Window ultrasound device (DEVICE).
Who is sponsoring clinical trial NCT02814721?
This trial is sponsored by Henry Ford Health System, which has 234 total clinical trials registered on ClinicalTrials.gov.
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