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İn This Study, Patients Undergoing Bariatric Surgery Will be Divided Into Two Groups. The Control Group Will Receive Normal-flow, While the Study Group Will Receive Low-flow Inhalational Anesthesia. The Aim is to Compare the Incidence of Postop Atelectasis-between the Two Groups Using USG Evaluation

Not Applicable
Not yet recruiting
Conditions
Ultrasonography
Atelectasis
Pulmonary Complications
Registration Number
NCT07041567
Lead Sponsor
Istanbul University
Brief Summary

This study is a clinical trial and its purpose is to evaluate the effect of low and normal flow anesthesia on atelectasis formation in patients undergoing bariatric surgery by ultrasonography.

In this study, lung ultrasounds and respiratory function tests will be performed on volunteers before and after surgery. These procedures are completely painless and safe.

No invasive procedure will be performed in the study; the methods used do not pose any additional risk other than existing treatment procedures.

Detailed Description

Not available

Recruitment & Eligibility

Status
NOT_YET_RECRUITING
Sex
All
Target Recruitment
60
Inclusion Criteria
  • Will undergo Sleeve Gastrectomy surgery;
  • 18-65 years old
  • ASA III patients.
Exclusion Criteria
  • Patients who do not give consent
  • Patients with ASA 4 and above
  • Those with serious respiratory comorbidities (interstitial lung disease, serious permanent lung diseases)
  • Uncontrolled Hypertension, Diabetes Mellitus
  • Under 18 and over 65 years of age
  • Chronic renal failure, Liver failure
  • CHF (EF<30) will not be included in the study

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
the atelectasis rate with the Lung Ultrasound score (AUS score).8 months
Secondary Outcome Measures
NameTimeMethod
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