Effect of Total Intravenous Anesthesia and Balanced Anesthesia on Postoperative Lung Function
NCT ID: NCT00706277
Last Updated: 2009-02-10
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
PHASE4
60 participants
INTERVENTIONAL
2008-06-30
2008-12-31
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.
Short Life Agents in Balanced Anesthesia on Obstructive Sleep Apnea Syndrome
NCT02717780
Interaction of Sevoflurane Propofol and Remifentanil in Anesthesia for Laparoscopic Surgery
NCT02457442
Sevoflurane, Propofol, Postoperative Pain
NCT01437462
Study of Anaesthesia Costs and Recovery Profiles
NCT02920749
Inflammatory Response Secondary Using Intravenous Anesthesia Versus Inhalation Anesthesia With Halogenated Agents
NCT02168751
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
TREATMENT
TRIPLE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
TIVA
patients receiving total intravenous anesthesia (TIVA)
propofol
propofol 2mg/kg for induction of anesthesia; followed by propofol 6 mg/kg/hour
remifentanil
remifentanil 0,25mcg/kg/hour
balanced
patients receiving balanced anesthesia
propofol
propofol 2mg
fentanyl
fentanyl 100mcg
Sevoflurane/Nitrous Oxide
maintenance of anesthesia with sevoflurane and nitrous oxide
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
propofol
propofol 2mg/kg for induction of anesthesia; followed by propofol 6 mg/kg/hour
propofol
propofol 2mg
remifentanil
remifentanil 0,25mcg/kg/hour
fentanyl
fentanyl 100mcg
Sevoflurane/Nitrous Oxide
maintenance of anesthesia with sevoflurane and nitrous oxide
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* BMI normal
Exclusion Criteria
* Nicotine abuse
18 Years
60 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Medical University Innsbruck
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
TILAK A-6020 Innsbruck, Anichstr. 35 AUSTRIA
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Arnulf Benzer, MD
Role: PRINCIPAL_INVESTIGATOR
TILAK Hospitals
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
TILAK Hospitals
Innsbruck, , Austria
Countries
Review the countries where the study has at least one active or historical site.
References
Explore related publications, articles, or registry entries linked to this study.
Gunnarsson L, Lindberg P, Tokics L, Thorstensson O, Thorne A. Lung function after open versus laparoscopic cholecystectomy. Acta Anaesthesiol Scand. 1995 Apr;39(3):302-6. doi: 10.1111/j.1399-6576.1995.tb04066.x.
Regli A, von Ungern-Sternberg BS, Reber A, Schneider MC. Impact of spinal anaesthesia on peri-operative lung volumes in obese and morbidly obese female patients. Anaesthesia. 2006 Mar;61(3):215-21. doi: 10.1111/j.1365-2044.2005.04441.x.
Natalini G, Franceschetti ME, Pletti C, Recupero D, Lanza G, Bernardini A. Impact of laryngeal mask airway and tracheal tube on pulmonary function during the early postoperative period. Acta Anaesthesiol Scand. 2002 May;46(5):525-8. doi: 10.1034/j.1399-6576.2002.460509.x.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
2007-007161-25
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.