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
16 participants
OBSERVATIONAL
2016-12-31
2017-12-31
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.
The Effects of Sevoflurane and Desflurane Used in Low-Flow Anesthesia on Thiol Disulfide Homeostasis
NCT06810453
The Effect of Sevoflurane and Desflurane on Clara Cell Protein on the Lung
NCT04645316
Desflurane and Sevoflurane Minimal Flow Anesthesia on Recovery and Anesthetic Depth
NCT05024084
Low-Flow Desflurane vs Sevoflurane: Impact on Physiology and Recoveryand Recovery Profiles in Adult ENT Surgery
NCT07016308
The Relationship of Sevoflurane Consumption With Metabolic Age
NCT06018597
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
All collection will assess with gas chromatography.
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_CONTROL
PROSPECTIVE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
two lung ventilation of Sevoflurane
In GroupSa, 1,5 % sevoflurane will be apply continuously and blood samples will be taken at intervals of 10 minutes starting from the 40th minute.
Sevoflurane
Measurement of blood desflurane level during one lung ventilation
one lung ventilation of Sevoflurane
In GroupSa, 1,5 % sevoflurane will be apply continuously and first samples will taken at the 40. minutes and collection of blood samples will be continue at intervals of 10 minutes after one lung ventilation started.
Sevoflurane
Measurement of blood desflurane level during one lung ventilation
two lung ventilation of Desflurane
In GroupSa, 6 % desflurane will be apply continuously and blood samples will be taken at intervals of 10 minutes starting from the 40th minute.
Desflurane
Measurement of blood desflurane level during one lung ventilation
one lung ventilation of desflurane
In GroupSa, 6 % desflurane will be apply continuously and first samples will taken at the 40. minutes and collection of blood samples will be continue at intervals of 10 minutes after one lung ventilation started.
Desflurane
Measurement of blood desflurane level during one lung ventilation
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Sevoflurane
Measurement of blood desflurane level during one lung ventilation
Desflurane
Measurement of blood desflurane level during one lung ventilation
Other Intervention Names
Discover alternative or legacy names that may be used to describe the listed interventions across different sources.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
Exclusion Criteria
* Patients who taken inotropic agent
25 Years
65 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Cukurova University
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
ebru biricik
MD, Anesthesiology specialist
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Ebru Biricik, MD
Role: PRINCIPAL_INVESTIGATOR
Cukurova University
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Ebru Biricik
Adana, In the USA Or Canada, Please Select..., Turkey (Türkiye)
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.
One lung ventilation
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.