Actively Recruiting
Inhalational Agents Versus Dexmedetomidine for Maintenance of General Anesthesia
Led by Bakirkoy Dr. Sadi Konuk Research and Training Hospital · Updated on 2026-01-23
150
Participants Needed
1
Research Sites
74 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The climate crisis and environmental pollution are escalating day by day, making the reduction of carbon footprints increasingly important both on an individual and industrial level. Inhalational anesthetic agents are widely used in daily anesthesia practice. However, some of these agents are released into the environment either unchanged or as metabolic by-products. It can take hundreds of years for these substances to be fully eliminated from nature. Therefore, there is a growing interest in identifying alternative anesthetic agents that are fully metabolized, do not produce waste, have a shorter duration of action, and pose less harm to ecosystems. Recent clinical studies have shown that dexmedetomidine, when administered intraoperatively via infusion without a loading dose and in combination with inhalational agents, provides more stable hemodynamics and results in a shorter postoperative recovery period. Commonly used as a long-term sedative agent in intensive care units, dexmedetomidine has gained popularity in the intraoperative setting due to its stable hemodynamic profile, low incidence of withdrawal symptoms, and faster recovery. In this study, it is aimed to demonstrate the potential use of dexmedetomidine-whose pharmacodynamic and pharmacokinetic properties are well-known to experienced anesthesiologists-as an alternative to inhalational anesthetic agents for the maintenance of anesthesia, particularly in the geriatric patient population.
CONDITIONS
Official Title
Inhalational Agents Versus Dexmedetomidine for Maintenance of General Anesthesia
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age 39 years or older
- Classified as ASA physical status II-IV
- Scheduled for elective endoscopic urological surgery (e.g., URS, TUR-B, PCNL, TUR-P)
- Scheduled for postoperative follow-up in the Post-Anesthesia Care Unit (PACU)
- Ability to provide written informed consent
You will not qualify if you...
- Need to convert to open surgery during the perioperative period
- Decline to participate in the study
- Presence of neuropsychiatric disorders such as dementia, Parkinson's disease, epilepsy, or history of head trauma
- History of alcohol or substance abuse
- Use of psychoactive medications
- Inability to communicate adequately for any reason
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Bakirkoy dr. Sadi Konuk
Istanbul, Istanbul, Turkey (Türkiye), 34140
Actively Recruiting
Research Team
N
NALAN SAYGİ EMİR
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
2
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