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NCT07097662Completed

Evaluation of the Effectiveness of Oxygen Reserve Index Monitoring During Pre-oxygenation in Obese Patients

Source: ClinicalTrials.gov · Last updated 31 Jul 2025

Brief summary (registry, in English)

In obese patients, the risk of perioperative complications such as rapid desaturation, atelectasis, difficult mask ventilation, difficult intubation, and hypoxia is higher compared to the normal population. Therefore, preoxygenation is even more critical in the obese patient group. In clinical practice, ETO2 is used as a practical indicator to evaluate sufficient oxygenation during preoxygenation. The Oxygen Reserve Index (ORiⓇ) is a new oxygenation monitoring parameter that is continuously and non-invasively measured by a specialized pulse oximetry device (Masimo, Irvine, CA).The primary objective of the investigators was to observe the correlation between ORIⓇ monitoring and ETO₂ during preoxygenation in obese patients.The secondary objective of the investigators was to evaluate the correlation of ORIⓇ with SpO₂ and PaO₂ in this patient population.

Status (registry)
Completed
Study type
Observational
Enrollment
60 (actual)
First submitted
17 Jul 2025
Start date
Feb 2024
Primary completion date
Jul 2024
Lead sponsor
Irem Caner
Diseases
Obesity
NCT number
NCT07097662

What you commit to

  • Study type: Observational
  • Participants enrolled: 60
  • From Feb 2024 to the primary completion date, Jul 2024
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Those receiving home oxygen therapy

Other illness

  • Psychiatric disorders
  • Severe cardiac arrhythmias
  • Chronic obstructive pulmonary disease (COPD)

Lab values

  • Patients with an ejection fraction below 30%

Other

  • Patients with ASA physical status classification IV-V,
  • Patients requiring supraglottic airway devices, and emergency cases

Who the study is looking for

  • Patients with a body mass index (BMI) \>35 kg/m² scheduled for elective surgery
  • ASA (American Society of Anesthesiologists) physical status classification I-III
  • Patients aged 18 years and older

Age in the registry: 18 years to 75 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Kocaeli University
Coordinator of this site? Confirm its status
KocaeliTurkey (Türkiye)Unknown status

This page is information, not medical advice. Discuss any trial with your doctor.