Anesthetic Techniques Impact on Oxidative Stress in VATS
This study aims to evaluate how different anesthesia techniques affect oxidative stress levels in patients undergoing video-assisted thoracic surgery, by measuring specific markers in the blood.
Total Intravenous Anesthesia (TIVA) Group
+ Balanced Anesthesia (BAL) Group
+ Combined Intravenous Volatile Anesthesia
Treatment Study
Summary
Study start date: December 1, 2025
Actual date on which the first participant was enrolled.This study is examining how different types of anesthesia affect oxidative stress during lung surgery that involves breathing through only one lung at a time. Oxidative stress is a condition that can cause damage to the body and is a concern during surgeries that involve reintroducing air into a previously non-ventilated lung. The study is focused on patients undergoing video-assisted thoracoscopic surgery, a less invasive type of lung surgery, and aims to find out which anesthetic technique—Total Intravenous Anesthesia (TIVA), Combined Intravenous-Volatile Anesthesia (CIVA), or Balanced Anesthesia (BAL)—is the most effective in reducing oxidative stress and preserving oxygen levels. By evaluating these techniques, the research hopes to improve patient safety and outcomes during such surgeries. Participants in the study will be randomly assigned to one of three anesthesia groups: TIVA, CIVA, or BAL. Each group will receive specific combinations of medications to maintain anesthesia, and their effects will be monitored throughout the surgery. Blood samples will be collected at three key moments: before anesthesia starts, before switching back to normal two-lung ventilation, and 30 minutes after resuming two-lung ventilation. These samples will help measure levels of oxidative stress markers like Malondialdehyde, Superoxide Dismutase, and others. The study will also track heart rate, blood pressure, and other vital signs to assess the overall effects of the anesthesia. Results will be analyzed to determine which method best minimizes oxidative stress and improves surgery outcomes.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.60 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Treatment Study
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Any sex
Biological sex of participants that are eligible to enroll.From 18 to 65 Years
Range of ages for which participants are eligible to join.Healthy volunteers not allowed
If individuals who are healthy and do not have the condition being studied can participate.Criteria
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.3 intervention groups are designated in this study
This study does not include a placebo group
Treatment Groups
Group I
ExperimentalGroup II
ExperimentalGroup III
ExperimentalStudy Objectives
Primary Objectives
Secondary Objectives
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 1 location