Correlation of PaCO2 to the Inspired and Expired Oxygen Gradient
NCT ID: NCT01513213
Last Updated: 2017-01-24
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
65 participants
OBSERVATIONAL
2011-10-31
2016-12-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Studying Physiological and Anatomical Cerebral Effects of Carbon Dioxide and Tilt
NCT02493985
Impact of NOS, COX, and ROS Inhibition on Cerebral Blood Flow Regulation
NCT03066115
Sympathetic Transduction in Obesity-associated Hypertension (OB-HTN)
NCT04838678
Neuroimaging During Pure Oxygen Breathing
NCT03268590
Cerebral Blood Flow and Metabolism During Hypoxia and Endotoxemia
NCT00332267
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
CASE_ONLY
CROSS_SECTIONAL
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Scheduled for surgical procedure that will last at least 2 hours.
* Arterial cannulation is planned because of either the complexity of the surgery or patient comorbidity.
* At least two arterial blood gas analyses are planned during the surgery.
Exclusion Criteria
18 Years
65 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Swedish Medical Center
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Arthur M Lam, MD, FRCPC
Role: PRINCIPAL_INVESTIGATOR
Swedish Medical Center
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Swedish Medical Center
Seattle, Washington, United States
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
5119S-11
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.