Prediction of Weaning Outcomes by Using Rate of Change of Rapid Shallow Breathing Index

This study has been terminated.
Sponsor:
Information provided by:
Atlantic Health System
ClinicalTrials.gov Identifier:
NCT00366197
First received: August 17, 2006
Last updated: January 15, 2014
Last verified: January 2014

August 17, 2006
January 15, 2014
January 2005
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Complete list of historical versions of study NCT00366197 on ClinicalTrials.gov Archive Site
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Prediction of Weaning Outcomes by Using Rate of Change of Rapid Shallow Breathing Index
Prediction of Weaning Outcomes by Using Rate of Change of Rapid Shallow Breathing Index

This trial examines weaning outcomes using the rapid shallow breathing index rate.

We hypothesize that the trend of the Rapid Shallow Breathing Index or RSBI rate, is a better predictor of weaning outcome than the RSBI as a single value during the weaning trial. patients are recruited during a weaning trial on t-piece and the RSBI during what the RSBI is measured periodically. The outcome is ventilatory status at 24 hours after the weaning trial.

Observational
Time Perspective: Prospective
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Non-Probability Sample

Male and Female

Rapid Shallow Breathing
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*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Terminated
100
July 2008
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Inclusion Criteria:

  • Requires need of mechanical ventilation for > 48 hours with a tube size no smaller than 7.5

Exclusion Criteria:

  • Healthy volunteers
Both
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No
Contact information is only displayed when the study is recruiting subjects
United States
 
NCT00366197
Rapid Shallow Breathing Index
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Atlantic Health System
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Principal Investigator: Stanley Fiel, MD Atlantic Health
Principal Investigator: Harris Rana, MD Atlantic Health
Principal Investigator: Salvatore Ruggiero, MD Atlantic Health
Principal Investigator: Erwin Oei, MD Atlantic Health
Atlantic Health System
January 2014

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP