Effect of Perioperative IV Ibuprofen on Cerebral Oxygenation and Postoperative Cognition During One-Lung Ventilation

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-75
SponsorOndokuz Mayıs University

About this trial

This study compares the effects of ibuprofen administered during surgery and within the first 24 hours after surgery, versus no ibuprofen, on cerebral oxygenation, postoperative changes in consciousness (postoperative delirium and cognitive dysfunction), length of stay in the intensive care unit, and the incidence of postoperative pain, nausea, vomiting, and pruritus in patients undergoing lung lobectomy or segmentectomy using a closed (video-assisted) method (VATS - video-assisted thoracoscopic surgery), in whom one-lung ventilation is applied.

The aim of this study is to evaluate the effects of ibuprofen on cerebral oxygenation, postoperative cognitive changes, and delirium in patients undergoing one-lung ventilation.

Eligibility criteria

Qualifiers

Patients aged 18-75 years

American Society of Anesthesiologists (ASA) Physical Status Classification System I-III

Patients scheduled for lobectomy or segmentectomy via Video-Assisted Thoracic Surgery (VATS ) with one-lung ventilation

New York Heart Association (NYHA) class I-II

Disqualifiers

Patients younger than 18 years or older than 75 years

History of alcohol or substance abuse

Patients with chronic NSAID use and/or NSAID use within the last 30 days, or NSAID allergy

Allergy to other drugs used in the study (e.g., bupivacaine)

Trial design

Treatments tested in this trial

  • ibuprofen

Treatment groups

54 Participants
are divided into 2 treatment groups

Locations

This trial has no locations

Sponsors and collaborators