Rapid Shallow BreathingNCT00366197
Prediction of Weaning Outcomes by Using Rate of Change of Rapid Shallow Breathing Index
An observational study of Rapid Shallow Breathing, run by Atlantic Health System at 1 site in United States.
Trial summary
This trial examines weaning outcomes using the rapid shallow breathing index rate. Read more about this study
- Who is it for?
- Any age
- Conditions the study is for
- Rapid Shallow Breathing
- How many people
- 100 participants
- Where
- 1 siteUnited States
- Study dates
- Jan 2005to Jul 2008
- Phase
- Observational
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages Any age
- All sexes
- No healthy volunteers
- Child, Adult, Older adult
Study population: Male and Female
Who may be able to join
- Requires need of mechanical ventilation for > 48 hours with a tube size no smaller than 7.5
Who cannot join
- Healthy volunteers
Trial locations and contacts
1 site in 1 country.
United States1 site
Morristown Memorial Hospital
Morristown, New Jersey, 07962
About this study
This trial examines weaning outcomes using the rapid shallow breathing index rate.
Read the detailed 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.
- Conditions
- Rapid Shallow Breathing
- Keywords
- Rapid Shallow Breathing Index, Mechanical Ventilation
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted21 Aug 2006 (estimated)
- Study startJan 2005
- Study completionJul 2008
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Rapid Shallow BreathingStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Time perspective
- Prospective
- Enrolment
- 100 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Atlantic Health System
- Sponsor type
- University, hospital or other
- Investigators
- Stanley Fiel, MD, Principal investigator, Atlantic Health SystemHarris Rana, MD, Principal investigator, Atlantic Health SystemSalvatore Ruggiero, MD, Principal investigator, Atlantic Health SystemErwin Oei, MD, Principal investigator, Atlantic Health System
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT00366197
- Sponsor's protocol ID
- Rapid Shallow Breathing Index
- Status last verified
- Jan 2014
- First submitted
- 17 Aug 2006
- Last updated
- 16 Jan 2014
- Results posted
- No
Study at a glance
From the registry record, last updated by the sponsor on 16 Jan 2014. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Prediction of Weaning Outcomes by Using Rate of Change of Rapid Shallow Breathing Index
- ClinicalTrials.gov ID
- NCT00366197
- Acronym / sponsor ID
- Rapid Shallow Breathing Index
- Conditions
- Rapid Shallow Breathing
- Keywords
- Rapid Shallow Breathing Index, Mechanical Ventilation
- Study type
- Observational
- Recruitment status
- Terminated
- Enrolment
- 100 participants (estimated)
- Lead sponsor
- Atlantic Health SystemUniversity, hospital or other
- Study start
- Jan 2005
- Study completion
- Jul 2008 (actual)
- First posted
- 21 Aug 2006 (estimated)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
This trial examines weaning outcomes using the rapid shallow breathing index rate.
Detailed 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.
Study design
- Time perspective
- Prospective
Who may qualify
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Child, Adult, Older adult
- Study population
- Male and Female
Key inclusion criteria (1 listed)
- Requires need of mechanical ventilation for > 48 hours with a tube size no smaller than 7.5
Key exclusion criteria (1 listed)
- Healthy volunteers
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Primary outcome
Not reported in the source record.
Results and safety
The study was stopped early. Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 16 Jan 2014.
Related trials for Rapid Shallow Breathing
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Combined RSBI, TOF, and BIS for Prediction of Extubation Success
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RecruitingObservational study
D-RSBI Versus RSBI for Predicting Weaning Success in COPD Patients
Chronic Obstructive Pulmonary Disease (COPD), Mechanical Ventilator Weaning
Not yet recruitingObservational study
Comparison of Diaphragm Ultrasound and RSBI for Predicting Weaning Success in Mechanically Ventilated ICU Patients
Ventilator Weaning, Mechanical Ventilation
Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Stanley Fiel, MD principal investigator
Atlantic Health System
Harris Rana, MD principal investigator
Atlantic Health System
Salvatore Ruggiero, MD principal investigator
Atlantic Health System
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Rapid Shallow Breathing, run by Atlantic Health System at 1 site in United States.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 1 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: stopped early, as of the sponsor's last update on 16 Jan 2014. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study was stopped early. Results are not available in the source record.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 16 Jan 2014.