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Clinical Trials in Turkey / NCT07100860
Recruiting Observational

The Effect of Single Lung Ventilation Duration on Postoperative Pulmonary Complications in Thoracic Surgery

NCT07100860 · tracked via the Priya Life Science Turkey tracker
Phase
Observational
Started
2025-01-01
Last updated
2025-12-18

Condition(s) studied

Postoperative Pulmonary ComplicationsOne Lung VentilationArdsPostoperative Pulmonary Atelectasis

Investigational drug(s) / intervention(s)

One-Lung ventilation

One-Lung ventilation: In this observational study, the naturally occurring duration of intraoperative single-lung ventilation (SLV) during thoracic surgery will be recorded. No intervention is applied or modified for research purposes. The exposure of interest is the total duration (in minutes) of SLV, which will be timed from initiation to termination during surgery. This variable will be analyzed in relation to postoperative pulmonary complications.

Study summary

This observational study investigates the relationship between the duration of single-lung ventilation (SLV) and the incidence of postoperative pulmonary complications (PPCs) such as pneumonia, pneumothorax, hemothorax, acute lung injury, and acute respiratory distress syndrome (ARDS) in adult patients undergoing thoracic surgery. A total of 134 patients aged 18-85 years, scheduled for thoracic surgery requiring SLV, will be monitored. Data including SLV duration, perioperative parameters, and postoperative pulmonary outcomes will be analyzed.

Eligibility

Sex
ALL
Min age
18 Years
Max age
85 Years
Healthy volunteers
No
Inclusion Criteria: Age ≥18 years Undergoing thoracic surgery OLV planned during the procedure Exclusion Criteria: Pediatric patients Patients not requiring OLV Previous thoracic surgery

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Hazal Ekin GÜRAN AYTUĞ Ankara Ankara Recruiting

More Dr Abdurrahman Yurtaslan Ankara Oncology Training and Research Hospital trials in Turkey

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 NCT07100860 on ClinicalTrials.gov ↗ ← All trials in Turkey