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Clinical Trials in Turkey / NCT07363681
Recruiting Not applicable

Inhalational Agents Versus Dexmedetomidine for Maintenance of General Anesthesia

NCT07363681 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2024-10-01
Last updated
2026-01-23

Condition(s) studied

Ureterorenoscopic LithotripsyTransurethral Resection of the BladderPercutaneous NephrolithotomyTransurethral Resection of the Prostate

Investigational drug(s) / intervention(s)

Dexmedetomidine + RemifentanilAll Dexmedetomidine trials (145) →All Remifentanil trials (17) →Desflurane + RemifentanilAll Desflurane trials (7) →All Remifentanil trials (17) →

Dexmedetomidine + Remifentanil: Anesthesia Protocol All patients will receive the same standardized induction regimen consisting of fentanyl (1 μg/kg), propofol (1 mg/kg), and rocuronium (0.5 mg/kg). Following induction, maintenance of general anesthesia will differ according to group allocation: In Group DR, anesthesia maintenance will be provided with dexmedetomidine administered as a continuous infusion without a loading dose, combined with remifentanil infusion. Remifentanil infusion rates will be adjusted as clinically required to maintain adequate hemodynamic stability and surgical anesthesia depth

Desflurane + Remifentanil: The investigators will administer desflurane combined with remifentanil for general anesthesia maintenance in this group.

Study summary

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.

Eligibility

Sex
ALL
Min age
39 Years
Max age
99 Years
Healthy volunteers
Accepted
Inclusion Criteria * Age ≥ 39 years * 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 Exclusion Criteria * Requirement for conversion to open surgery during the perioperative period * Patients who decline to participate in the study * Presence of neuropsychiatric disorders (e.g., 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

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Bakirkoy dr. Sadi Konuk Istanbul Istanbul Recruiting

More Bakirkoy Dr. Sadi Konuk Research and Training Hospital trials in Turkey

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07363681 on ClinicalTrials.gov ↗ ← All trials in Turkey