Actively Recruiting

Phase Not Applicable
Age: 39Years - 99Years
All Genders
Healthy Volunteers
NCT07363681

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

Age: 39Years - 99Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

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
Not Eligible

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

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Trial Site Locations

Total: 1 location

1

Bakirkoy dr. Sadi Konuk

Istanbul, Istanbul, Turkey (Türkiye), 34140

Actively Recruiting

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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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