Inhalation Anesthesia

2

Review clinical trials related to Inhalation Anesthesia. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Effect of Combined Intravenous-Inhalational Anesthesia (CIVIA) on Postoperative Recovery Patterns.

This study was planned as a single-center, prospective, randomized trial. Adult patients undergoing elective spinal surgery lasting longer than three hours, performed in a neurosurgery operating room, will be evaluated. Patients managed with three different anesthesia methods currently used will be examined for recovery patterns: 1. Total intravenous anesthesia (TIVA), 2. TIVA Combined anesthesia with sevoflurane and intravenous agents (sevoflurane-CIVIA), 3. TIVA Combined anesthesia with desflurane and intravenous agents (desflurane-CIVIA). Recovery patterns include; extubation time, eye opening time, emergence agitation, postoperative nausia and vomiting and postoperative recovery unit discharge time.

Participants needed: 210
Trial details
Phase: Phase 4Age: 18+Biological sex: AllType: InterventionalSponsor: Kocaeli City HospitalUpdated: Aug 14, 2025Locations: 1
Eligibility criteria

Scheduled for spine surgery [+5]

Emergency surgeries [+4]

Status: Recruiting

Wash-in Period in Patients Undergoing Low Flow Anesthesia

Volunteers above the age of 18 and below the age of 60 who agreed to participate in the study were not exposed to any interventional intervention other than those routinely applied to the patient during and after the administration of the clinical standard anesthesia protocol. The value indicating the brain's response to hypnotic substances, the vapor concentration in the lung alveoli and the minimum amount of anesthesia gas used will be recorded at certain times. The aim of the researchers in the study was to observe the effect of two different fresh gas flow rates on the amount and cost of waste gas released into the atmosphere.

Participants needed: 40
Trial details
Age: 18-60Biological sex: AllType: ObservationalSponsor: Serkan UckunUpdated: May 16, 2025Locations: 3
Eligibility criteria

ASA I-II risk group patients Duration of surgery between 2 hours and 4 hours, ca...

Patient refusal to participate in the study [+16]