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NCT00785252 Clinical Trial

EZIO Compared to Central Venous Lines for Emergency Vascular Access

Catheters, Indwelling Clinical Trial

Official title:
Randomized Study of the EZIO Compared to Central Venous Lines Used for Emergency Vascular Access

Clinical Trial Details — Status: Withdrawn

Administrative data
NCT number NCT00785252
Other study ID # 100731 (completed)
Secondary ID
Status Withdrawn
Phase N/A
First received
Last updated
Start date September 2008
Est. completion date September 2010

Study information
Verified date September 2021
Source National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Multicenter randomized study to compare powered intraosseous access to standard central line access for the administration of fluids and drugs for patients in the Emergency Dept.

Recruitment information / eligibility
Status Withdrawn
Enrollment 0
Est. completion date September 2010
Est. primary completion date September 2010
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: Over 18 years old Requires central access after peripheral access attempts have failed or are not otherwise feasible Exclusion Criteria: Fracture in target bone Not able to sign informed consent Excessive tissue or absence of adequate anatomical landmarks Known or suspected coagulopathies Pregnancy Patients in custody Patients with suspected great vessel injury Not fluid in English

Study Design

Related Conditions & MeSH terms

Intervention

Device:
• Powered Intraosseous device (EZIO)
EZIO
• standard central line
placement of a central line

Locations
Country Name City State
United States Dept of Emergency Medicine, The George Washington University Medical Center Washington District of Columbia

Sponsors (2)
Lead Sponsor Collaborator
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) Vidacare Corporation

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary Time taken to place the device ED visit
Secondary Incidence of complications ED visit
Secondary Costs for each of the two methods Ed visit
See also
  Status Clinical Trial Phase
Completed NCT03351725 - Peripheral Venous Catheter Colonization Study
Completed NCT00272623 - Seldinger Technique Versus Venous Cut-Down for Placement of Totally Implantable Venous Access Ports N/A
Completed NCT00001518 - A Randomized Evaluation of the Effect of Routine Normal Saline Flush Versus Heparinized Saline Solution in Groshong and Groshong PICC Catheters N/A
Completed NCT00073515 - Trial of a Novel Fibrinolytic (Alfimeprase) to Clear Thrombosed Vascular Access Devices Phase 2

External Links