Postoperative SpO₂/FiO₂ Ratio and Analgesic Methods in Laparoscopic Surgery

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorIstinye University

About this trial

This prospective observational study aims to evaluate the association between postoperative oxygenation, assessed by the SpO₂/FiO₂ ratio, and body mass index (BMI), STOP-BANG score, and postoperative analgesic methods in patients undergoing elective laparoscopic cholecystectomy in the reverse Trendelenburg position. Postoperative SpO₂ and FiO₂ values will be recorded within the first postoperative hour, and the SpO₂/FiO₂ ratio will be calculated. Analgesic techniques applied as part of routine clinical practice will be documented. The study does not involve any additional intervention beyond standard care. The findings are expected to contribute to a better understanding of factors associated with early postoperative oxygenation and hypoxemia risk.

Eligibility criteria

Qualifiers

Age ≥ 18 years

Patients who provide written informed consent

ASA physical status I-III

Patients undergoing elective laparoscopic cholecystectomy

Disqualifiers

Age < 18 years

Refusal or inability to provide informed consent

ASA physical status IV or higher

Known chronic respiratory diseases (e.g., asthma, COPD)

Trial design

Treatments tested in this trial

  • Standard of Care

Treatment groups

100 Participants
are divided into 2 treatment groups

Sponsors and collaborators