Environmental Oxygen Levels During Artificial Ventilation and Oxygen Therapy
NCT ID: NCT06718361
Last Updated: 2025-05-18
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
50 participants
OBSERVATIONAL
2025-02-01
2025-04-30
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
The study aims to performed a series of measurement of the oxygen concentration in the environment around the patient with different airway management used and ventilation provided.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
ORI to Reduce Hyperoxia After Out Hospital Cardiac Arrest
NCT03653325
Rapid Prehospital ACcess to ECPR in Prague
NCT06789978
Automatic Ventilation in Prehospital Resuscitation on OHCA
NCT06067204
Optimization of Transport and Use of a Mobile ECMO Team in Patients With Sudden Cardiac Arrest in the Moravian-Silesian Region
NCT07009652
Treatment Outcome in Patients After eCPR
NCT07031466
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.
COHORT
PROSPECTIVE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
O2 mask
Delivering oxygen via face mask with different oxygen flow (5, 10, 15 l/min).
Oxygen levels measurement (%)
Measuring levels of oxygen in the environment around the patient in %.
Bag mask ventilation
Delivering oxygen via bag mask ventilation
Oxygen levels measurement (%)
Measuring levels of oxygen in the environment around the patient in %.
Supraglotic airway
Delivering oxygen via laryngeal mask with bag or mechanical ventilation
Oxygen levels measurement (%)
Measuring levels of oxygen in the environment around the patient in %.
Orotracheal intubation
Delivering oxygen via orotracheal tube with bag or mechanical ventilation
Oxygen levels measurement (%)
Measuring levels of oxygen in the environment around the patient in %.
High-Flow Nasal Oxygenation
Oxygen delivery via high-flow nasal oxygenation
Oxygen levels measurement (%)
Measuring levels of oxygen in the environment around the patient in %.
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Oxygen levels measurement (%)
Measuring levels of oxygen in the environment around the patient in %.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
Exclusion Criteria
* situation not allowing measurement
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Charles University, Czech Republic
OTHER
David Peran, PhD, FERC
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
David Peran, PhD, FERC
Deputy director
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
David Peran, PhD
Role: PRINCIPAL_INVESTIGATOR
Zdravotnicka Zachranna Sluzba Karlovarskeho Kraje, P.O.
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
FNKV University Hospital
Prague, , Czechia
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.
Robertshaw H, McAnulty G. Ambient oxygen concentrations during simulated cardiopulmonary resuscitation. Anaesthesia. 1998 Jul;53(7):634-7. doi: 10.1046/j.1365-2044.1998.410-az0512.x.
Theodorou AA, Gutierrez JA, Berg RA. Fire attributable to a defibrillation attempt in a neonate. Pediatrics. 2003 Sep;112(3 Pt 1):677-9. doi: 10.1542/peds.112.3.677. No abstract available.
Miller PH. Potential fire hazard in defibrillation. JAMA. 1972 Jul 10;221(2):192. No abstract available.
Cantello E, Davy TE, Koenig KL. The question of removing a ventilation bag before defibrillation. J Accid Emerg Med. 1998 Jul;15(4):286. doi: 10.1136/emj.15.4.286. No abstract available.
Barker SJ, Polson JS. Fire in the operating room: a case report and laboratory study. Anesth Analg. 2001 Oct;93(4):960-5. doi: 10.1097/00000539-200110000-00031.
Hummel RS 3rd, Ornato JP, Weinberg SM, Clarke AM. Spark-generating properties of electrode gels used during defibrillation. A potential fire hazard. JAMA. 1988 Nov 25;260(20):3021-4.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
ZZSKVK-01-2024
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.