← Eichor
Study identifier: NCT07363681 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Inhalational Agents Versus Dexmedetomidine for Maintenance of General Anesthesia

Condition: Ureterorenoscopic Lithotripsy · Transurethral Resection of the Bladder · Percutaneous Nephrolithotomy  ·  Sponsor: Bakirkoy Dr. Sadi Konuk Research and Training Hospital

PhaseNA
Planned participants150
Who can joinAll sexes, 39 Years to 99 Years
Healthy volunteersYes

About this study

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.

This description comes directly from the study's public registry record.

Talk to the study team

NALAN SAYGİ EMİR  ·  00905422363672  ·  nasaemir@hotmail.com

Always discuss trial participation with your own doctor first.

Locations (1)

Bakirkoy dr. Sadi KonukIstanbul, Istanbul, Turkey (Türkiye)Recruiting

Follow this study

Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.

We email about this public record only. Unsubscribe anytime with one click. Never medical advice.

Is this your study? This page was generated automatically from the public registry record. Sponsors can claim it — free — to add branding and verified contact routing. Claim this page →

This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.

Source record: clinicaltrials.gov/study/NCT07363681