Actively Recruiting

Age: 18Years - 60Years
All Genders
NCT06967948

Wash-in Period in Patients Undergoing Low Flow Anesthesia

Led by Serkan Uckun · Updated on 2025-05-16

40

Participants Needed

3

Research Sites

33 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

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.

CONDITIONS

Official Title

Wash-in Period in Patients Undergoing Low Flow Anesthesia

Who Can Participate

Age: 18Years - 60Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients aged 18 to 60 years
  • ASA I-II risk group patients
  • Surgery duration between 2 and 4 hours
  • Cases receiving general anesthesia
Not Eligible

You will not qualify if you...

  • Patient refusal to participate
  • Under 18 years old or BMI over 40
  • Use of invasive mechanical ventilator support in the last month
  • Chemotherapy or radiotherapy within the last 2 months
  • Severe lung disease (COPD, asthma, pulmonary infection, bronchiectasis, or recent need for ventilation or steroid therapy)
  • Known severe pulmonary hypertension
  • Smoke poisoning (carbon monoxide, cyanide)
  • Alcohol or acetone poisoning
  • Malignant hyperthermia
  • Intracranial tumor
  • Hemodynamic instability or shock
  • Neuromuscular disease
  • Conditions causing increased intracranial or intraocular pressure
  • Severe cardiac arrhythmias or ejection fraction below 30%
  • Severe peripheral arterial disease
  • Liver or kidney dysfunction

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 3 locations

1

Balıkesir University Health Practice and Research Hospital Operating Room

Balıkesir, Turkey (Türkiye)

Actively Recruiting

2

Balıkesir University Health Practice and Research Hospital

Balıkesir, Turkey (Türkiye)

Actively Recruiting

3

Balıkesir University Health Practice and Research Hospital

Balıkesir, Turkey (Türkiye)

Actively Recruiting

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Research Team

S

Serkan Uçkun, assistant professor

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

2

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