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

Rapid Shallow Breathing Clinical Trial

Official title:

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

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT00366197
• Other study ID #: Rapid Shallow Breathing Index
• Status: Terminated
• Phase: Phase 0
• First received: August 17, 2006
• Last updated: January 15, 2014
• Start date: January 2005
• Est. completion date: July 2008

Study information

• Verified date: January 2014
• Source: Atlantic Health System
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Institutional Review Board
• Study type: Observational

Clinical Trial Summary

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

Description:

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.

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 100
• Est. completion date: July 2008
• Accepts healthy volunteers: No
• Gender: Both
• Age group: N/A and older

Eligibility

Inclusion Criteria:

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

Exclusion Criteria:

• Healthy volunteers

Study Design

Time Perspective: Prospective

Related Conditions & MeSH terms

• Rapid Shallow Breathing
• Respiratory Aspiration

Locations

Country	Name	City	State
United States	Morristown Memorial Hospital	Morristown	New Jersey

Sponsors (1)

Lead Sponsor	Collaborator
Atlantic Health System

Country where clinical trial is conducted

United States,