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Clinical Trials in Turkey / NCT07404267
Starting soon Not applicable

Oxygen Reserve Index-Guided Oxygen Titration During Surgery in the Beach Chair Position

NCT07404267 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2026-02-15
Last updated
2026-02-11

Condition(s) studied

HyperoxemiaIntraoperative Oxygen TherapyBeach Chair PositionCerebral Oxygenation

Investigational drug(s) / intervention(s)

ORi-Guided FiO₂ TitrationSpO₂-Guided FiO₂ Titration

ORi-Guided FiO₂ Titration: Inspiratory oxygen fraction (FiO₂) will be adjusted throughout surgery using combined Oxygen Reserve Index (ORi) and peripheral oxygen saturation (SpO₂) monitoring. FiO₂ will be titrated to maintain ORi values between 0.2 and 0.5, with reassessment every 2-3 minutes.

SpO₂-Guided FiO₂ Titration: FiO₂ will be adjusted to maintain SpO₂ at or above 98% throughout surgery.

Study summary

This study aims to evaluate whether guidance by the Oxygen Reserve Index (ORi) improves inspiratory oxygen fraction (FiO₂) titration compared with conventional pulse oximetry (SpO₂)-guided oxygen administration in adult patients undergoing surgery in the beach chair position.

Oxygen therapy is routinely used during general anesthesia to prevent hypoxemia; however, excessive oxygen administration may result in hyperoxia, which has been associated with adverse cardiovascular and pulmonary effects. Standard pulse oximetry may not adequately detect hyperoxia when oxygen saturation values are high.

In this prospective comparative study, patients will receive oxygen titration guided either by SpO₂ alone or by combined ORi and SpO₂ monitoring. The primary outcome is the incidence of intraoperative hyperoxemia, assessed by arterial blood gas analysis. Secondary outcomes include intraoperative oxygenation parameters and hemodynamic variables.

Eligibility

Sex
ALL
Min age
18 Years
Max age
65 Years
Healthy volunteers
Accepted
Inclusion Criteria: * Adult patients aged 18 to 65 years * American Society of Anesthesiologists (ASA) physical status I-III * Scheduled for elective orthopedic surgery in the beach chair position * Body mass index (BMI) \<35 kg/m² * Ability to provide written informed consent Exclusion Criteria: * Age \<18 or ≥65 years * Finger deformities preventing the use of Oxygen Reserve Index (ORi) monitoring * Severe anemia (hemoglobin \<8 g/dL) * Pregnancy * Refusal or inability to provide informed consent * History of stroke or significant vascular pathology * Severe cardiac or respiratory disease

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Istanbul Provincial Health Directorate Fatih Sultan Mehmet Training and Research Hospital Istanbul Turkey (Türkiye)

More Fatih Sultan Mehmet Training and Research Hospital trials in Turkey

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07404267 on ClinicalTrials.gov ↗ ← All trials in Turkey