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Clinical Trials in Turkey / NCT07654153
Starting soon Observational

Surgical Positions and Postoperative Atelectasis: A Lung Ultrasound Study

NCT07654153 · tracked via the Priya Life Science Turkey tracker
Phase
Observational
Started
2026-07-20
Last updated
2026-07-21

Condition(s) studied

Lung UltrasoundAtelectasis

Investigational drug(s) / intervention(s)

lung ultrasound

lung ultrasound: Lung Ultrasound (LUS) Protocol: The LUS evaluation will be performed by Dr. Burak Ağar using a Mindray ultrasound device \[Device brand/model and probe type, e.g., 3.5-5 MHz convex or 7-12 MHz linear probe\]

Study summary

The aim of this study is to prospectively evaluate the effect of surgical position on the development of postoperative atelectasis in patients undergoing surgery in supine, prone, lateral decubitus, and lithotomy positions using lung ultrasonography (LUS), and to investigate whether there is a difference between these positions.

Eligibility

Sex
ALL
Min age
18 Years
Max age
80 Years
Healthy volunteers
Accepted
Inclusion Criteria: * Being between 18-80 years of age * Having ASA I-III status * Planning elective surgery under general anesthesia * Agreeing to participate in the study and signing the consent form Exclusion Criteria: * Patients requiring emergency surgery * Patients with ASA IV or higher * Presence of a known serious preoperative lung disease (COPD, Asthma, Pneumonia, Pleural effusion, Pneumothorax, Interstitial lung disease, Bronchiectasis, etc.) * History of neuromuscular disease * Body Mass Index (BMI) \> 35 kg/m² (Morbid obesity) * Presence of chest wall deformity or skin lesions that would obstruct LUS imaging * Cases with an operative duration of less than 60 minutes or more than 300 minutes * Patients with a history of thoracotomy, sternotomy, or prior open thoracic surgery * Patients with alcohol or drug dependence * Patients with significant anemia * Patients who are pregnant or lactating * Patients who develop laryngospasm following extubation * Refusal to provide consent or inability to cooperate

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Sivas Cumhuriyet University Sivas Sivas

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Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07654153 on ClinicalTrials.gov ↗ ← All trials in Turkey