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NCT04039490 · ClinicalTrials.gov registry record · NA
Novel Device for Ultrasound-guided Pediatric Vessel Cannulations
A NA study of Clinical Procedures Which Require Vessel Cannulations in Pediatric Patients, sponsored by Clear Guide Medical.
- Recruiting
- Registry status
- NA
- Development phase
- 60
- Enrollment target
- 1
- Study location
NCT04039490 is a NA study of Clinical Procedures Which Require Vessel Cannulations in Pediatric Patients that is actively recruiting participants, run by Clear Guide Medical. The registered enrollment target is 60 participants. The trial reports 1 study location across 1 state.
The verdict
NCT04039490, a NA study of Clinical Procedures Which Require Vessel Cannulations in Pediatric Patients, is actively recruiting participants, sponsored by Clear Guide Medical.
- RECRUITING
- Registry status
- NA
- Development phase
- 60 participants
- Enrollment target
- 1
- Study location
Study Summary
Clinical Trial to investigate whether the use of a novel device to be used in conjunction with ultrasound in pediatric vessel cannulations is superior to ultrasound-only pediatric vessel cannulations in terms of number of cannulation attempts.
Conditions Studied
Interventions
- DEVICE SCENERGY
Study Locations (1)
District of Columbia
- Children's National Medical Center - Washington D.C.
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 60 participants |
| Start Date | 2024-02-06 |
| Est. Completion | 2025-08-31 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT04039490
The ClinicalTrials.gov registry entry for NCT04039490 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 60 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Clear Guide Medical, which has 5 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Clinical Procedures Which Require Vessel Cannulations in Pediatric Patients appearing as the primary indexed condition, and to 1 intervention - of which SCENERGY is the first listed.
NCT04039490 reports 1 study location spanning 1 distinct geographic area - top geographies include District of Columbia.
Frequently Asked Questions
What is clinical trial NCT04039490 about?
NCT04039490 is a clinical study titled "Novel Device for Ultrasound-guided Pediatric Vessel Cannulations". Clinical Trial to investigate whether the use of a novel device to be used in conjunction with ultrasound in pediatric vessel cannulations is superior to ultrasound-only pediatric vessel cannulations in terms of number of cannulation attempts.
What is the current status of trial NCT04039490?
This trial is currently recruiting. It is a NA study. The enrollment target is 60 participants. The study started on 2024-02-06. Estimated completion is 2025-08-31.
What conditions does trial NCT04039490 study?
This clinical trial studies the following conditions: Clinical Procedures Which Require Vessel Cannulations in Pediatric Patients.
What interventions are being tested in trial NCT04039490?
The interventions under investigation include: SCENERGY (DEVICE).
Who is sponsoring clinical trial NCT04039490?
This trial is sponsored by Clear Guide Medical, which has 5 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT04039490 being conducted?
This trial has 1 study location across District of Columbia. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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