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COMPLETED
NCT07525661
NA

Perioperative Hyperoxia vs Normoxia Biomarker Trial

Sponsor: Istanbul University

View on ClinicalTrials.gov

Summary

This single-center randomized interventional study evaluated the biological effects of two perioperative oxygen strategies in adults undergoing elective laparoscopic lower abdominal surgery under standardized general anesthesia. Participants were assigned to receive either normoxia (FiO2 0.35) or hyperoxia (FiO2 0.80) after intubation and throughout the intraoperative period. The study assessed perioperative changes in circulating biomarkers related to pulmonary epithelial stress, endothelial glycocalyx injury, oxidative stress, and inflammation, together with blood gas and hemodynamic parameters. The study was completed before registration and is being registered retrospectively.

Official title: Effects of Perioperative Hyperoxia Versus Normoxia on Pulmonary, Endothelial, and Inflammatory Biomarkers in Elective Laparoscopic Lower Abdominal Surgery

Key Details

Gender

All

Age Range

18 Years - 70 Years

Study Type

INTERVENTIONAL

Enrollment

76

Start Date

2017-07-01

Completion Date

2019-02-01

Last Updated

2026-04-13

Healthy Volunteers

No

Interventions

OTHER

Perioperative Oxygen Strategy - Normoxia

Normoxia arm: FiO2 0.35 Intervention started immediately after intubation and maintained intraoperatively

OTHER

Perioperative Oxygen Strategy-Hyperoxia

Hyperoxia arm: FiO2 0.80 Intervention started immediately after intubation and maintained intraoperatively

Locations (1)

Istanbul University, Istanbul Faculty of Medicine

Istanbul, Turkey (Türkiye)