ClinicalTrials.gg
CompletedNCT07158073Updated Sep 8, 2025

Effect of ORI-guided Oxygen Titration on Oxidative Stress in Rhinoplasty Surgery

An interventional study of FiO₂ titration, under the guidance of ORI and Conventional oxygen administration in Rhinoplasty, Oxidative Stress and Hyperoxia, sponsored by Dr. Lutfi Kirdar Kartal Training and Research Hospital. Completed at 1 site in Turkey (Türkiye). Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2025-09-08.

Sponsored by Dr. Lutfi Kirdar Kartal Training and Research Hospital · Not applicable, Interventional, and Prevention

From the registry’s dates

  • Registered 4 years 5 months after the study started (first participant enrolled Mar 2021, registered Aug 2025).
Phase
Not applicable
Study type
Interventional
Enrollment
60
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

The aim of this study is to evaluate whether the use of Oxygen Reserve Index (ORİ) can prevent hyperoxia in patients undergoing rhinoplasty surgery and whether it can reduce oxidative stress caused by hyperoxia.

Read the detailed description

ORI is a continuous, non-invasive parameter provided by new-generation pulse oximeters utilizing multi-wavelength pulse oximetry technology. ORI serves as an important monitoring tool for detecting both hyperoxemia and desaturation in patients with decreased PaO₂ levels. Studies have demonstrated that ORI provides values within a range of 0 to 1, and an ORI value of 0 corresponds to a PaO₂ level between 80 and 125 mmHg.

Oxygen is commonly used in clinical practice to prevent or treat hypoxia; however, excessive use may lead to oxidative stress. Oxidative stress is defined as a disruption of the oxidative balance resulting from an increased generation of reactive oxygen species (ROS) during cellular metabolism and an insufficient level of antioxidants to detoxify them. ROS are formed by the reaction of molecular oxygen with H₂O, the most stable form of oxygen. In this reaction, the stepwise addition of electrons to molecular oxygen (O₂) leads to the formation of superoxide anion (O₂ˉ), hydrogen peroxide (H₂O₂), and hydroxyl radical (-OH). Among these, the hydroxyl radical is the most reactive form of oxygen radicals.

Although ROS are essential for normal cellular functions such as intracellular signaling and defense against external threats, their excessive production can lead to molecular and cellular dysfunction. Excessive ROS attack nucleotide bases in nucleic acids, amino acid side chains in proteins, and double bonds in unsaturated fatty acids, resulting in oxidative stress that damages DNA, RNA, proteins, and lipids, leading to structural and metabolic changes in cells.

The primary aim of the investigators in this study is to determine whether ORI-guided oxygen titration during rhinoplasty surgery can help prevent hyperoxia and reduce oxidative stress compared with conventional oxygen therapy. To evaluate oxidative stress, thiol-disulfide balance and ischemia-modified albumin (IMA) levels will be assessed in the participants.

02

Conditions studied

  • Rhinoplasty
  • Oxidative Stress
  • Hyperoxia
  • Oxygen Reserve Index

Browse trials for

Keywords

  • Rhinoplasty surgery
  • Oxygen Reserve Index
  • Oxidative Stress
  • Hyperoxia
03

In context

Hyperoxia

115 studies on the registry are indexed under Hyperoxia; 13 are open to participants now.

This study's enrollment of 60 is above the median of 48 across 82 interventional studies indexed under Hyperoxia.

Browse Hyperoxia studies →

Lead sponsor

Dr. Lutfi Kirdar Kartal Training and Research Hospital is the lead sponsor of 78 studies on the registry; 9 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • classified as I or II

Exclusion criteria

Exclusion Criteria:

  • under 18 years of age
  • greater than II
  • Mallampati score of 3 or 4
  • findings suggestive of difficult intubation during physical examination
  • any pathological findings on chest X-ray evaluation (e.g., pleural effusion, nodular density increase, emphysema, atelectasis, calcification, mediastinal widening, or infiltration)
  • a history of circulatory disorders
  • hematocrit or values outside the normal range (Hemoglobin: 12-16 g/dL for males, 11-14 g/dL for females; Hematocrit: 36-48% for males, 33-42% for females)
  • a known to any anesthetic agent to be used in the study.
Terms in these criteria, in plain language(3)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

ASA physical status

The anaesthetists’ scale of health before surgery: I is healthy, II has a mild illness that is under control, III a severe one, IV a severe illness that is a constant threat to life. V and VI are used for the critically ill and for organ donors.

Hemoglobin (Hb)

The protein in red blood cells that carries oxygen. A low level is anaemia, which can cause tiredness and breathlessness. Measured in g/dL or g/L (9 g/dL is 90 g/L).

Hypersensitivity

An allergy, or another reaction of the immune system, to a substance. “Hypersensitivity to the study drug” means a known allergic reaction to it — not every side effect a medicine can have.

05

Study design

Phase
Not applicable
Primary purpose
Prevention
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Quadruple (Participant, Care provider, Investigator, Outcomes assessor)
Enrollment
60 participants (actual)

Study arms

  • Active comparator
    ORI group (Group R)

    Patients in Group R received ORI monitoring in addition to intraoperative standart monitoring (ECG, pulse oximetry, non-invasive arterial blood pressure). For this purpose, an ORI sensor (RD Rainbow SET sensor, Masimo Corp., Irvine, CA, USA) was placed on the fourth finger of the upper extremity where there was no blood pressure cuff. The sensor was wrapped to prevent exposure to light and connected to an oximeter device (Raical-7® Pulse CO-Oximater®, Masimo Corp., Irvine, CA, USA).In Group R, mask ventilation was administered with 50% oxygen. FiO₂ was titrated between 30% and 50% under the guidance of ORI and SpO₂ values. Accordingly, if SpO₂ was ≥ 98%, FiO₂ was reduced in 5% increments to a minimum of 30%, aiming to achieve an ORI value of 0 or as close to 0 as possible.

    Device: FiO₂ titration, under the guidance of ORI

  • Active comparator
    Control group (Group C)

    Patients in Group C received only standard monitoring. Mask ventilation was administered with 100% oxygen. FiO₂ was maintained at 50% throughout the surgery, provided that SpO₂ remained ≥ 98%.

    Device: Conventional oxygen administration

Interventions

  • DeviceFiO₂ titration, under the guidance of ORI

    In Group R, FiO₂ was titrated between 30% and 50% under the guidance of ORI and SpO₂ values. Accordingly, if SpO₂ was ≥ 98%, FiO₂ was reduced in 5% increments to a minimum of 30%, aiming to achieve an ORI value of 0 or as close to 0 as possible.

  • DeviceConventional oxygen administration

    In Group C, FiO₂ was maintained at 50% throughout the surgery, provided that SpO₂ remained ≥ 98%.

06

What researchers measure

Primary outcomes

  1. Change in thiol-disulfide balance.

    Plasma native thiol, total thiol, and disulfide levels will be measured. The disulfide-to-thiol ratio will be used as a marker of oxidative stress. Unit of Measure: µmol/L

    Time frame: preoperative to end of surgery (before awakening)

  2. Change in ischemia-modified albumin (IMA) levels.

    Serum IMA levels will be measured as an indicator of oxidative stress. IMA reflects modification of the N-terminal region of albumin by reactive oxygen species (ROS). Unit of Measure: Absorbance Units (ABS units)

    Time frame: preoperative-end of surgery (before awakening)

Secondary outcomes

  1. PaO₂ levels.

    To compare intraoperative PaO₂ changes between ORI and Control groups. Arterial blood gas samples were obtained from all patients after intubation, at the 2nd hour of surgery, and at the end of the procedure before awakening.

    Time frame: From baseline (after intubation) to end of surgery (before awakening)

07

Study locations

1 site
  • Kartal Dr. Lütfi Kırdar City Hospital
    Istanbul, kartal 34862, Turkey (Türkiye)
08

References and documents

Publications

  • Karakasoglu R, Geyik FD, Cevik BE, Saracoglu KT. The effect of oxygen reserve index guided oxygen titration on oxidative stress in rhinoplasty surgery: a randomized controlled trial. BMC Anesthesiol. 2025 Nov 4;25(1):542. doi: 10.1186/s12871-025-03424-0. PubMed 41188744 ↗

Individual participant data

Plan to share: No

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 8, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07158073
Lead sponsor
Dr. Lutfi Kirdar Kartal Training and Research Hospital
Responsible party
Recep Karakaşoğlu (MD, Dr. Lutfi Kirdar Kartal Training and Research Hospital) — Principal investigator
First posted
Sep 5, 2025
Start date
Mar 1, 2021
Primary completion
Aug 20, 2021
Completion
Aug 30, 2021
Last update
Sep 8, 2025

Study contacts

Banu E Çevik, MD
study director · University of Health Sciences, Kartal Dr. Lütfi Kırdar City Hospital
Fatih D Geyik, MD
principal investigator · University of Health Sciences, Kartal Dr. Lütfi Kırdar City Hospital
Kemal T Saraçoğlu, MD
principal investigator · University of Health Sciences, Kartal Dr. Lütfi Kırdar City Hospital
Recep karakaşoğlu, MD
principal investigator · University of Health Sciences, Kartal Dr. Lütfi Kırdar City Hospital

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Sep 2025. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion