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NCT01866475 · ClinicalTrials.gov registry record · NA
Continuous Intraosseous Vascular Access Over 48 Hours
A NA study of Intraosseous Vascular Access, sponsored by Vidacare Corporation.
- Completed
- Registry status
- NA
- Development phase
- 127
- Enrollment target
- 1
- Study location
NCT01866475 is a NA study of Intraosseous Vascular Access that has completed, run by Vidacare Corporation. The registered enrollment target is 127 participants. The trial reports 1 study location across 1 state.
The verdict
NCT01866475, a NA study of Intraosseous Vascular Access, has completed, sponsored by Vidacare Corporation.
- COMPLETED
- Registry status
- NA
- Development phase
- 127 participants
- Enrollment target
- 1
- Study location
Study Summary
A prospective study to determine the safety of intraosseous (IO) access for a period up to 48 hours in healthy adult volunteers and volunteers with a history of mild to moderate renal disease and/or controlled diabetes.
Conditions Studied
Interventions
- DEVICE EZ-IO
Study Locations (1)
Texas
- ICON Early Phase Services - San Antonio
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 127 participants |
| Start Date | 2014-11 |
| Est. Completion | 2016-07 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01866475
The ClinicalTrials.gov registry entry for NCT01866475 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 127 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Vidacare Corporation, which has 11 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Intraosseous Vascular Access appearing as the primary indexed condition, and to 1 intervention - of which EZ-IO is the first listed.
NCT01866475 reports 1 study location spanning 1 distinct geographic area - top geographies include Texas.
Frequently Asked Questions
What is clinical trial NCT01866475 about?
NCT01866475 is a clinical study titled "Continuous Intraosseous Vascular Access Over 48 Hours". A prospective study to determine the safety of intraosseous (IO) access for a period up to 48 hours in healthy adult volunteers and volunteers with a history of mild to moderate renal disease and/or controlled diabetes.
What is the current status of trial NCT01866475?
This trial is currently completed. It is a NA study. The enrollment target is 127 participants. The study started on 2014-11. Estimated completion is 2016-07.
What conditions does trial NCT01866475 study?
This clinical trial studies the following conditions: Intraosseous Vascular Access.
What interventions are being tested in trial NCT01866475?
The interventions under investigation include: EZ-IO (DEVICE).
Who is sponsoring clinical trial NCT01866475?
This trial is sponsored by Vidacare Corporation, which has 11 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT01866475 being conducted?
This trial has 1 study location across Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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