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
- Conditions
- UltrasonographyAtelectasisPulmonary 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
- Will undergo Sleeve Gastrectomy surgery;
- 18-65 years old
- ASA III patients.
- 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
Name Time Method the atelectasis rate with the Lung Ultrasound score (AUS score). 8 months
- Secondary Outcome Measures
Name Time Method
Related Research Topics
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