Wash-in Period in Patients Undergoing Low Flow Anesthesia
ConditionInhalation Anesthesia
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-60
SponsorSerkan Uckun
About this trial
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.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
ASA I-II risk group patients Duration of surgery between 2 hours and 4 hours, cases with general anesthesia
Disqualifiers
Patient refusal to participate in the study
Under 18 years old BMI>40
Patients receiving invasive mechanical ventilator support in the last 1 month
Patients who have received chemotherapy or radiotherapy in the last 2 months
Trial population
Male or female Between 18-60 years of age ASA I-II risk group patients with general anesthesia Duration of surgery between 2 hours and 4 hours
Trial design
Design model
Case-control
Time perspective
Prospective
Treatments tested in this trial
Not listed
Trial groups
40 Participants
are grouped into 2 trial groupsGroup A: 1 lt/min
Group B: 4 lt/min
Trial outcomes
Primary outcomes
1
Demographic data
Demographic data such as age (years), height (cm), weight (kg) and gender (male/female) of the volunteer patients will be analyzed to see if they are similar for both study groups.
Time frame
preoperative2
Duration of surgery
It will be examined whether the duration of surgery (minutes) is similar for volunteer patients
Time frame
During the period of operation (2-4 hours)3
Duration of anesthesia
It will be examined whether the duration of anesthesia (minutes) is similar for volunteer patients
Time frame
During the period of operation (2-4 hours)4
Heart rate
We will examine whether there is a difference in heart rate (beats/minute) values recorded at 5-minute intervals in the first half hour and at 15-minute intervals thereafter in volunteer patients
Time frame
During the period of operation (2-4 hours)Sponsors and contacts
Click on the lead sponsor to view all of their trials.
Serkan Uckun
Lead sponsor
Balikesir University
Sponsor institution
Source ClinicalTrials.gov