Status:
COMPLETED
Assess the Ability of Electrical Cardiometry to Trend Hemodynamic Variables During Dexmedetomidine Sedation
Lead Sponsor:
Boston Children's Hospital
Conditions:
Cardiac Output
Sedation
Eligibility:
All Genders
1-18 years
Brief Summary
The aim of the study is to investigate the use of a new FDA-approved non-invasive bio-impedance cardiac monitor, ICON, to detect hemodynamic effects during sedation in children undergoing radiology pr...
Eligibility Criteria
Inclusion
- All pediatric patients (1 month to 18 years of age)
- Eligible for Radiology Sedation Service for CT scan and Nuclear Medicine
- Scan procedure
Exclusion
- Pacemakers and Vagus Nerve Stimulator
- Mitral or Aorta Valve Dysfunction
- Dextrocardia
- Second or Third degree heart block
- Current diagnosis of Cardiac, Pulmonary, Hepatic or Renal Failure
- Current diagnosis of pulmonary masses/tumor/pleural effusions/pneumonia/edema
- Pericardial effusion
- Concomitant use of hypertension medications including ACE inhibitors, beta receptor and calcium channel blockers.
- Large Implanted Metallic Devices (including orthodontic braces, spine rods, plates and screws)
- Allergy to device electrodes
Key Trial Info
Start Date :
September 1 2009
Trial Type :
OBSERVATIONAL
Allocation :
ACTUAL
End Date :
September 1 2011
Estimated Enrollment :
17 Patients enrolled
Trial Details
Trial ID
NCT01001533
Start Date
September 1 2009
End Date
September 1 2011
Last Update
January 5 2017
Active Locations (1)
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1
Children Hospital Boston
Boston, Massachusetts, United States, 02115