Apneic Oxygenation

2

Review clinical trials related to Apneic Oxygenation. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

Effect of Continuous Supraglottic Oxygen Insufflation Via Video Laryngoscope Blade on Apneic Oxygenation During Tracheal Intubation Under General Anesthesia

This study is a prospective, randomized controlled clinical trial aimed at investigating the efficacy and safety of a novel oxygenating video laryngoscope blade during apneic oxygenation for intubation under general anesthesia. Hypoxemia is prone to occur during anesthesia induction, which can lead to severe complications. Apneic oxygenation is an important method to prolong the safe apnea time, but existing oxygen delivery modalities have limitations in applicability. Although the laryngeal oxygen delivery approach combined with video laryngoscopy has theoretical advantages, clinical evidence is insufficient. Therefore, this study was conducted.

Participants needed: 150
Trial details
Age: 18-75Biological sex: AllType: InterventionalSponsor: Affiliated Hospital of Jiaxing UniversityUpdated: Jun 23, 2026
Eligibility criteria

Patients aged between 18 and 75 years, with ASA physical status I to III, and sc...

cardiac disease (ischaemic heart disease, heart failure [NYHA ≥2 ],current arrhy... [+4]

Status: Not yet recruiting

Oxygen Reserve Index (ORi) in Identifying Desaturation

This randomized clinical trial investigates whether Oxygen Reserve Index (ORi) monitoring enables earlier detection of impending hypoxemia compared with conventional pulse oximetry during apneic intermittent ventilation in adult patients undergoing endolaryngeal surgery under general anesthesia. By providing continuous, noninvasive assessment of oxygen reserve in the hyperoxic range, ORi may offer an earlier warning of oxygen depletion before peripheral oxygen saturation declines. The study compares time to reventilation thresholds, arterial blood gas parameters, and perioperative respiratory outcomes between ORi-guided and standard SpO₂-guided monitoring strategies.

Participants needed: 80
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Istanbul UniversityUpdated: Feb 17, 2026Locations: 1
Eligibility criteria

Age 18 years or older [+4]

Age under 18 years [+4]