ClinicalTrials.gov record
Terminated No phase listed Observational Results available

Observational Study of Rapid Sequence Intubation Drug Delivery Using Intraosseous and Intravenous Access.

ClinicalTrials.gov ID: NCT01486407

Public ClinicalTrials.gov record NCT01486407. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced May 20, 2026, 7:27 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

An Observational Study of Intubating Conditions Comparing Intraosseous Vascular Access With Peripheral Intravenous Access for Drug Delivery in Rapid Sequence Intubation

Study identification

NCT ID
NCT01486407
Recruitment status
Terminated
Study type
Observational
Phase
Not listed
Lead sponsor
Vidacare Corporation
Industry
Enrollment
4 participants

Conditions and interventions

Conditions

Interventions

Not listed

Eligibility (public fields only)

Age range
Not listed
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jan 31, 2012
Primary completion
Nov 30, 2012
Completion
Nov 30, 2012
Last update posted
Jan 7, 2026

2012

United States locations

U.S. sites
2
U.S. states
1
U.S. cities
2
Facility City State ZIP Site status
Christus Spohn Hospital Corpus Christi Corpus Christi Texas 78405
Texas Tech University Health Science Center El Paso El Paso Texas 79905

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01486407, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jan 7, 2026 · Synced May 20, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01486407 live on ClinicalTrials.gov.

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