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Oxygen Reserve Index (ORi) in Identifying Desaturation

The Role of Oxygen Reserve Index (ORi) in Identifying Early Desaturation During Endolaryngeal Surgery: A Randomized Clinical Trial

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07415161
Enrollment
80
Registered
2026-02-17
Start date
2026-01-27
Completion date
2026-03-25
Last updated
2026-02-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Apneic Oxygenation, Endolarengeal Surgery, Oxygen Reserve Index

Keywords

oxygen reserve index, pulse oximetry, apneic ventilation

Brief summary

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.

Detailed description

This prospective, single-center, randomized clinical trial was designed to evaluate the role of the Oxygen Reserve Index (ORi) in the early detection of hypoxemia during apneic intermittent ventilation in adult patients undergoing elective endolaryngeal surgery under general anesthesia. Endolaryngeal procedures require shared airway management and frequently involve apneic periods, during which conventional pulse oximetry may fail to provide timely warning of declining oxygen reserves due to the plateau phase of the oxyhemoglobin dissociation curve. Eligible patients aged 18 years and older with ASA physical status I-III were randomly assigned to either an ORi-monitored group or a control group monitored with standard peripheral oxygen saturation (SpO₂). All patients underwent standardized anesthesia induction, preoxygenation, and apneic intermittent ventilation. In the ORi group, the threshold for resuming ventilation was defined as ORi reaching zero, whereas in the control group ventilation was resumed when SpO₂ decreased to 90%. The primary outcome was the time from the onset of apnea to the predefined reventilation threshold. Secondary outcomes included arterial blood gas parameters (pH, PaO₂, PaCO₂) at the time of reventilation, end-tidal carbon dioxide levels, perioperative lung ultrasound findings, post-anesthesia care unit length of stay, and postoperative respiratory outcomes. This study aims to determine whether ORi monitoring provides earlier and clinically meaningful warning of oxygen reserve depletion compared with conventional pulse oximetry, potentially improving patient safety during shared-airway surgery.

Interventions

PROCEDUREoxygen monitoring techniques

to determine whether ORi monitoring provides earlier and clinically meaningful warning of oxygen reserve depletion compared with conventional pulse oximetry, potentially improving patient safety during shared-airway surgery.

Sponsors

Istanbul University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Masking description

Masking Description

Intervention model description

Model Description

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Age 18 years or older * Scheduled for elective endolaryngeal surgery * Planned general anesthesia with apneic intermittent ventilation * American Society of Anesthesiologists (ASA) physical status I-III * Ability to provide written informed consent

Exclusion criteria

* Age under 18 years * Preoperative chronic hypoxemia (baseline SpO₂ \< 95%) * Patients transferred from the intensive care unit * ASA physical status IV or higher * Refusal or inability to provide informed consent

Design outcomes

Primary

MeasureTime frameDescription
Time to Reventilation ThresholdFrom the onset of apnea until the predefined reventilation threshold is reached during the intraoperative period (within minutes).Time from the onset of apnea to the predefined reventilation threshold, defined as Oxygen Reserve Index (ORi) reaching zero in the ORi group and peripheral oxygen saturation (SpO₂) decreasing to 90% in the control group, measured in seconds.

Secondary

MeasureTime frameDescription
Arterial Blood Gas Parameters at ReventilationFrom the onset of apnea until the predefined reventilation threshold is reached during the intraoperative period (within minutes).Arterial blood gas values including pH, partial pressure of oxygen (PaO₂), and partial pressure of carbon dioxide (PaCO₂) measured at the time of reventilation.
Perioperative Lung Ultrasound FindingsPreoperatively (before anesthesia induction) and postoperatively in the post-anesthesia care unit (within 1 hour after surgery).Change in lung ultrasound (LUS) B-line count between preoperative and postoperative assessments.
Postoperative Oxygenationpostoperatively in the post-anesthesia care unit (within 1 hour after surgery).Lowest peripheral oxygen saturation (SpO₂) recorded during PACU stay.
End-Tidal Carbon Dioxide (EtCO₂) LevelDuring the apneic period, measured at the time of reventilation during surgery.First recorded EtCO₂ value during apnea prior to reventilation.

Countries

Turkey (Türkiye)

Contacts

CONTACTDemet Altun, Prof
drdemetaltun@hotmail.com00905326811767
CONTACTece naz demir, resident
ecenazdemir95@gmail.com00905064524892
PRINCIPAL_INVESTIGATORece naz demir, resident

Istanbul University

STUDY_DIRECTORdemet altun, prof

Istanbul University

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 18, 2026