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Oxygen Reserve Index in Different Fresh Gas Flow

S

Sakarya University

Status

Completed

Conditions

Oxygen Reserve Index

Treatments

Device: Oxygen reserve index

Study type

Observational

Funder types

Other

Identifiers

NCT06649279
E16214662-050.01.04-8172-213

Details and patient eligibility

About

Our primary objective is to determine whether oxygen reserve index ORI can be a reliable and sensitive indicator of hypoxia and hyperoxia in low-flow anesthesia settings. Our secondary objective is to investigate the ORI changes during preoxygenation stage.

Enrollment

64 patients

Sex

All

Ages

18 to 75 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • ASA I-III patients
  • 18-75 years old
  • underwent general anesthesia
  • elective ear, nose and throat surgery, lasting longer than 60 minutes

Exclusion criteria

  • who did not consent to participate,
  • those with finger deformities
  • unregulated diabetes mellitus, severe heart, kidney, or liver failure, sensitivities to local anesthetics or opioids, those who were morbidly obese (BMI >40 kg/m²), and breastfeeding women.

Trial design

64 participants in 2 patient groups

Group H
Description:
High Flow Anesthesia Group
Treatment:
Device: Oxygen reserve index
Group M
Description:
Minimal Flow Anesthesia Group
Treatment:
Device: Oxygen reserve index

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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