The Clinical Value of Applying TOF and TcPO2 to Guide Elderly Patients Extubation
NCT ID: NCT02327910
Last Updated: 2016-03-23
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.
UNKNOWN
NA
300 participants
INTERVENTIONAL
2014-10-31
2017-01-31
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.
Cerebral Oximetry in Single Lung Ventilation Thoracic Surgery
NCT01866657
Assessment of Preoxygenation Strategies in the Prehospital Environment
NCT02694705
TCOT Effectiveness in Preventing Wound Infections in Perineal Resections
NCT02374294
End-tidal Oxygen Can Reliably Predict the Arterial Partial Pressure of Oxygen Among Emergency Department Patients
NCT03842306
Comparison of End-tidal Carbon Dioxide (ETCO2) Measured by Transportable Capnometer (EMMATM) and the Arterial pCO2 in General Anesthesia
NCT02184728
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.
RANDOMIZED
PARALLEL
PREVENTION
DOUBLE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Conventional group
Conventional group:The patients of conventional group were extubated when standard criteria were met;
No interventions assigned to this group
TOF group
TOF group: patients had a TOF ratio of greater than 0.90 as an additional extubation criterion;
TOF group
The patients of T group were extubated when TOF ratio greater than 0.9.
TOF unit TcPCO2 group
Qualitative TOF and transcutaneous partial pressure of carbon dioxide monitoring(Unite group):the patients of U group were extubated when TOF ratio greater than 0.9 and TcPCO2 recovery to preoprative(±5mmHg)
TOF unit TcPCO2 group
The patients of U group were extubated when TOF ratio greater than 0.9 and TcPCO2 recovery to preoprative(±5mmHg)
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
TOF unit TcPCO2 group
The patients of U group were extubated when TOF ratio greater than 0.9 and TcPCO2 recovery to preoprative(±5mmHg)
TOF group
The patients of T group were extubated when TOF ratio greater than 0.9.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
Exclusion Criteria
65 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Beijing Municipal Science & Technology Commission
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Zhaolei
The medical team leader
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
BeijingMSTC
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.