Viewing Study NCT01634867


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Study NCT ID: NCT01634867
Status: WITHDRAWN
Last Update Posted: 2014-12-23
First Post: 2012-07-02
Is NOT Gene Therapy: True
Has Adverse Events: False

Brief Title: Observational Study of Rapid Sequence Intubation (RSI) Drug Delivery Using Intraosseous (IO) and Intravenous (IV) Access in Pediatric Patients
Sponsor: Vidacare Corporation
Organization:

Study Overview

Official Title: A Pilot Study of Intubating Conditions Comparing Intraosseous Vascular Access With Peripheral Intravenous Access for Drug Delivery in Rapid Sequence Intubation Using Rocuronium as the Paralytic Agent
Status: WITHDRAWN
Status Verified Date: 2014-12
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: No subject enrollment.
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: This study will evaluate using intraosseous vascular access and intravenous vascular access to give pediatric patients the necessary medications to perform rapid sequence intubation, for patients with airway difficulties.
Detailed Description: None

Study Oversight

Has Oversight DMC: False
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: