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NCT06667401 · ClinicalTrials.gov registry record
Exploring the Efficacy of Assistive Artificial Intelligence for Ultrasound Guided Regional Anesthesia in Residency Training
A clinical trial, sponsored by Medical College of Wisconsin.
- Completed
- Registry status
- 20
- Enrollment target
NCT06667401 is a clinical trial that has completed, run by Medical College of Wisconsin. The registered enrollment target is 20 participants.
The verdict
NCT06667401 has completed, sponsored by Medical College of Wisconsin.
- COMPLETED
- Registry status
- 20 participants
- Enrollment target
Study Summary
The purpose of this study is to investigate the efficacy of a novel artificial intelligence (AI) device designed to assist in Ultrasound guided regional anesthesia (ScanNav Anatomy Peripheral Nerve Block; ScanNav), in the teaching and training of anesthesiology residents in the subspecialty of regional anesthesia.
Interventions
- DEVICE The ScanNav, a novel artificial intelligence device designed to assist in Ultrasound guided regional anesthesia
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 20 participants |
| Start Date | 2025-03-10 |
| Est. Completion | 2026-01-01 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06667401
The ClinicalTrials.gov registry entry for NCT06667401 describes a study currently listed as completed, categorized as an unspecified phase. The registered enrollment target is 20 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Medical College of Wisconsin, which has 447 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 1 intervention - of which The ScanNav, a novel artificial intelligence device designed to assist in Ultrasound guided regional anesthesia is the first listed.
NCT06667401 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT06667401 about?
NCT06667401 is a clinical study titled "Exploring the Efficacy of Assistive Artificial Intelligence for Ultrasound Guided Regional Anesthesia in Residency Training". The purpose of this study is to investigate the efficacy of a novel artificial intelligence (AI) device designed to assist in Ultrasound guided regional anesthesia (ScanNav Anatomy Peripheral Nerve Block; ScanNav), in the teaching and training of anesthesiology residents in the subspecialty of regio...
What is the current status of trial NCT06667401?
This trial is currently completed. The enrollment target is 20 participants. The study started on 2025-03-10. Estimated completion is 2026-01-01.
What interventions are being tested in trial NCT06667401?
The interventions under investigation include: The ScanNav, a novel artificial intelligence device designed to assist in Ultrasound guided regional anesthesia (DEVICE).
Who is sponsoring clinical trial NCT06667401?
This trial is sponsored by Medical College of Wisconsin, which has 447 total clinical trials registered on ClinicalTrials.gov.
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