Oxygen Saturation Alarms in the Neonatal Intensive Care Unit
NCT ID: NCT01085539
Last Updated: 2014-08-07
Study Results
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View full resultsBasic Information
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COMPLETED
50 participants
OBSERVATIONAL
2010-01-31
2010-06-30
Brief Summary
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Detailed Description
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This is an observational study of 50 infants at three hospitals in the United States. The observer will be an experienced nurse with comprehensive training to ensure consistency. The infants and clinical staff will be observed for four hours continuously. Observers will note the timing of alarms, response, interrupted clinical staff activities, and any clinical interventions, and timing of interventions. Clinical staff will also be questioned on whether the alarm was consistent with a desaturation event. Infant characteristics may affect the frequency of alarms. Data collected will include age, gender, weight, ethnicity, diagnosis, and medications.
This study will evaluate the proportion of nuisance alarms relative to the proportion of clinically relevant alarms. It will also evaluate the differences in alarm frequencies across infant characteristics and characterize nurse activities interrupted by the alarms.
Conditions
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Study Design
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CASE_ONLY
PROSPECTIVE
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
ALL
No
Sponsors
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Medtronic - MITG
INDUSTRY
Responsible Party
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Principal Investigators
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Roger Mecca, MD
Role: STUDY_CHAIR
Medtronic - MITG
Locations
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University of Alabama at Birmingham
Birmingham, Alabama, United States
Wake Forest University School of Medicine
Winston-Salem, North Carolina, United States
MetroHealth Medical Center
Cleveland, Ohio, United States
Countries
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Other Identifiers
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COV-M0-PO-A108
Identifier Type: -
Identifier Source: org_study_id
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