Low-Flow Desflurane Anesthesia and Its Effects on BIS and Postoperative Cognitive Functions
The Effects of Different Low-Flow Desflurane Anesthesia Strategies on Bispectral Index and Postoperative Cognitive Functions in Patients Undergoing Major Abdominal Surgery
1 other identifier
observational
72
1 country
1
Brief Summary
This study investigates the effects of low-flow desflurane anesthesia in adult patients undergoing major abdominal surgery. The researchers will examine whether different low-flow strategies: Cause differences in the Bispectral Index (BIS), which measures brain activity during anesthesia, Affect postoperative cognitive functions such as memory and attention. Participants will: Receive desflurane anesthesia during surgery, Have anesthesia delivered at different low-flow rates, Have their BIS values monitored throughout the operation, Complete tests after surgery to evaluate their cognitive functions. This research will help determine the safety of different low-flow strategies and their impact on patients' cognitive recovery after surgery.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for all trials
Started May 2025
Shorter than P25 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
May 15, 2025
CompletedFirst Submitted
Initial submission to the registry
October 1, 2025
CompletedFirst Posted
Study publicly available on registry
October 8, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 20, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
December 21, 2025
CompletedDecember 9, 2025
October 1, 2025
7 months
October 1, 2025
December 7, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Change from Baseline in Mini-Mental State Examination (MMSE) Score Postoperatively
Measure: Change in cognitive function assessed by the Mini-Mental State Examination (MMSE) Time Frame: From baseline (preoperative assessment) to postoperative assessment (within 24 hours after surgery) Description: The MMSE will be used to evaluate changes in cognitive function in patients receiving desflurane anesthesia at different low-flow rates. The primary endpoint is the difference between preoperative and postoperative MMSE scores.
From baseline (preoperative assessment, within 24 hours before surgery) to postoperative assessments at 24 hours and 7 days after surgery
Study Arms (1)
Group 1 :desflurane 0.5 L/min Group 2 :desflurane 1 L/min Group 3 : desflurane 1.5 L/min
This cohort includes adult patients undergoing major abdominal surgery whose general anesthesia is maintained with desflurane using different low-flow strategies. The main intervention of interest is the variation in fresh gas flow rates. Participants will be divided into three subgroups according to the applied flow rate: 0.5 L/min desflurane anesthesia 1.0 L/min desflurane anesthesia 1.5 L/min desflurane anesthesia During surgery, the depth of anesthesia will be continuously monitored using the Bispectral Index (BIS). Cognitive function will be assessed both preoperatively and postoperatively with the Mini-Mental State Examination (MMSE). This design will allow comparison of the effects of different low-flow strategies on intraoperative BIS values as well as on cognitive function changes before and after surgery.
Interventions
Routine anesthesia care (desflurane at different low-flow rates: 0.5, 1.0, 1.5 L/min); no intervention assigned as part of the study.
Eligibility Criteria
The study population will be recruited from patients undergoing elective major abdominal surgery at the Department of Anesthesiology and Reanimation, Ankara Dr Abdurrahman Yurtaslan Onkology Training and Research Hospital.
You may qualify if:
- Patients aged 18-75 years
- ASA physical status I-III
- Scheduled for elective major abdominal surgery
- Provided written informed consent
- Normal preoperative neurocognitive function
You may not qualify if:
- History of neurological or psychiatric disorders
- History of cognitive impairment
- Diagnosed hepatic or renal insufficiency
- Presence of other systemic diseases contraindicating anesthesia
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Dolunay ARIKlead
Study Sites (1)
Dr. Abdurrahman Yurtaslan Oncology Training and Research Hospital
Ankara, YENİMAHALLE, 06200, Turkey (Türkiye)
Related Publications (3)
Bingol Tanriverdi T, Tercan M, Gusun Halitoglu A, Kaya A, Patmano G. Comparison of the Effects of Low-flow and Normal-flow Desflurane Anaesthesia on Inflammatory Parameters in Patients Undergoing Laparoscopic Cholecystectomy. Turk J Anaesthesiol Reanim. 2021 Feb;49(1):18-24. doi: 10.5152/TJAR.2020.30. Epub 2020 Nov 30.
PMID: 33718901BACKGROUNDhttps://www.researchgate.net/publication/319617159_Low_flow_anesthesia_will_gain_eras_enhanced_recovery_after_surgery
BACKGROUNDBaum JA. Low-flow anesthesia: theory, practice, technical preconditions, advantages, and foreign gas accumulation. J Anesth. 1999;13(3):166-74. doi: 10.1007/s005400050050. No abstract available.
PMID: 14530937BACKGROUND
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR INVESTIGATOR
- PI Title
- Resident Doctor (Anesthesiology)
Study Record Dates
First Submitted
October 1, 2025
First Posted
October 8, 2025
Study Start
May 15, 2025
Primary Completion
December 20, 2025
Study Completion
December 21, 2025
Last Updated
December 9, 2025
Record last verified: 2025-10