- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01235650
Prevalence of Inadvertent Hyperventilation During Intraoperative Anesthetic Care
January 27, 2012 updated by: Joseph D. Tobias, Nationwide Children's Hospital
This is a retrospective chart review of patients undergoing spinal fusion surgery to see the prevalence of hyperventilation.
Study Overview
Status
Completed
Conditions
Detailed Description
Retrospective review of the operative schedules to identify patients who have undergone spinal fusion with placement of an arterial cannula for intermittent arterial blood gas analysis.
The intraoperative records will be retrospectively reviewed.
The following demographic data will be recorded: age, weight, gender, and co-morbid medical conditions.
Ventilatory parameters at the time of ABG analysis will include (respiratory rate and tidal volume).
ABG data will be collected.
Study Type
Observational
Enrollment (Actual)
160
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Spinal fusion patients
Description
Inclusion Criteria:
- Patients who underwent complex surgical procedures (spinal fusions) which necessitated arterial line placement and intermittent arterial blood gas analysis
Exclusion Criteria:
- None
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
---|
Spinal fusion
Patients who underwent complex surgical procedures (spinal fusions) which necessitated arterial line placement and intermittent arterial blood gas analysis
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Incidence of inadvertent hyperventilation
Time Frame: Day 1
|
Day 1
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
September 1, 2010
Primary Completion (Actual)
July 1, 2011
Study Completion (Actual)
July 1, 2011
Study Registration Dates
First Submitted
November 4, 2010
First Submitted That Met QC Criteria
November 4, 2010
First Posted (Estimate)
November 5, 2010
Study Record Updates
Last Update Posted (Estimate)
January 31, 2012
Last Update Submitted That Met QC Criteria
January 27, 2012
Last Verified
January 1, 2012
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- IRB10-00390
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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