Ultrasound for Postop Lung Issues in Low-Flow Anesthesia
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorAnkara Ataturk Sanatorium Training and Research Hospital
About this trial
Detecting possible atelectasis and other respiratory problems that may develop immediately after extubation via lung ultrasonography can reduce pulmonary complications by performing necessary interventions such as oxygen support, respiratory exercises, mobilization, and non-invasive mechanical ventilation applications at an early stage. In addition, although low-flow anesthesia is frequently used in daily anesthesia practice, publications showing the effects of its use in laparoscopic cholecystectomy operations on pulmonary complications are limited. On this occasion, this study can be presented as a contribution to the literature.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Patients with informed consent
Patients scheduled for laparoscopic cholecystectomy
Patients with a Body Mass Index between 18-35 kg/m²
Patients in the American Society of Anesthesiologist (ASA) 1-2-3 category
Disqualifiers
Patients with emergency surgery planned
Patients with ASA 4 and above
Patients with lung disease
Patients who have undergone thoracic surgery
Trial population
All cases that meet the inclusion and exclusion criteria will be included in the study. Patients will be taken to the operating room after being preoperatively evaluated in the observation room. The patient's anesthetic management will be provided by another anesthesiologist who is not participating in the study and is responsible for the patient. Intraoperative data will be obtained from the patient's anesthesia follow-up form and the records of the anesthesia machine. When the patients arrive in the recovery room, postoperative ultrasonographic measurements and other evaluations will be performed and noted. This group will include patients who received general anesthesia using low-flow techniques during the intraoperative period.
Trial design
Design model
Other
Time perspective
Prospective
Treatments tested in this trial
No-intervention
Other interventionNo interventions will be performed by the research team.
Treatment groups
110 Participants
are divided into 1 treatment groupGroup A: Low-Flow Anesthesia Group1 intervention
Trial outcomes
Primary outcomes
1
incidence of postoperative atelectasis
Incidence of postoperative atelectasis determined by lung ultrasonography in patients undergoing laparoscopic cholecystectomy with low-flow anesthesia
Time frame
1 hour peroperativelySecondary outcomes
1
incidence of other postoperative pulmonary complications
Other postoperative pulmonary complications that may develop and be detected by ultrasonography such as pneumothorax, pleural effusion, pulmonary edema
Time frame
1 hour peroperativelySponsors and contacts
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Source ClinicalTrials.gov