Effect of THRIVE During Apneic Oxygenation in General Anesthesia on Biomarkers
- Conditions
- AnesthesiaOxygen Toxicity
- Interventions
- Device: Endotracheal intubation and mechanical ventilationDevice: Apnoeic oxygenation using THRIVE
- Registration Number
- NCT03453294
- Lead Sponsor
- Karolinska University Hospital
- Brief Summary
Oxygenation with high-flow nasal cannula with 100% oxygen have now been evaluated in a number of studies and the data are convincing. The THRIVE technique is able to oxygenate patients safely and vital parameters has been shown to be stable. But it is of great importance to evaluate this new concept regarding other potential negative physiological aspects such as biological stress response detected by blood-bourne biomarkers before implementing it into clinical practice.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 30
- Adults, >18 years old.
- Laryngeal-surgery where apnea is of benefit for the surgeon (eg. intraoral or laryngeal surgery).
- Capable of understanding the study information and sign the written consent.
- American Society of Anaesthesiologist severity score >2
- New York Heart Association score >2
- Pacemaker or ICD.
- Body Mass Index >35
- Pregnancy
- Manifest cardiac failure or coronary disease
- Severe gastrointestinal reflux.
- Neuromuscular disorder
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Endotracheal intubation and mechanical ventilation Endotracheal intubation and mechanical ventilation Ventilation and oxygenation by an endotracheal tub and mechanical ventilation Apnoeic oxygenation using THRIVE Apnoeic oxygenation using THRIVE Oxygenation by apnoea oxygenation using THRIVE
- Primary Outcome Measures
Name Time Method Oxidative stress Up to 2 hours after start of intervention Biomarkers of oxidative stress such as Thiobarbituric acid reactive substances, Advanced Oxidation Protein Products,Reactive oxygen species and total antioxidant capacity in blood samples
- Secondary Outcome Measures
Name Time Method Inflammatory response Up to 2 hours after start of intervention Biomarkers of Inflammatory response in blood such as cytokines and interleukins
Biomarkers of cardiac damage Up to 2 hours after start of intervention Biomarkers of cardiac damage in blood such as troponin and ProBNP
Biomarkers of neuronal injury Up to 2 hours after start of intervention Biomarkers of neuronal injury and stress in blood such as S100 and Nuclear Serum Enolase
Biomarkers of kidney injury Up to 2 hours after start of intervention Biomarkers of kidney injury in blood such as creatinine
Markers of RNA damage Up to 2 hours after start of intervention Markers of RNA damage in blood
Trial Locations
- Locations (1)
Karolinska University Hospital
🇸🇪Stockholm, Sweden