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RecruitingNCT07100860Updated Dec 18, 2025

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

An observational study in Postoperative Pulmonary Complications, One Lung Ventilation and Ards, sponsored by Dr Abdurrahman Yurtaslan Ankara Oncology Training and Research Hospital. Recruiting at 1 site in Turkey (Türkiye). Open to participants aged 18 Years to 85 Years. Per ClinicalTrials.gov, last updated 2025-12-18.

Sponsored by Dr Abdurrahman Yurtaslan Ankara Oncology Training and Research Hospital · Observational

From the registry’s dates

  • Started Jan 2025; still recruiting 1 year 9 months later.
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
134
Ages
18 Years to 85 Years
Sex
All
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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.

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Conditions studied

  • Postoperative Pulmonary Complications
  • One Lung Ventilation
  • Ards
  • Postoperative Pulmonary Atelectasis

Keywords

  • postoperative pulmonary complications
  • one lung ventilation
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In context

Acute Lung Injury

989 studies on the registry are indexed under Acute Lung Injury; 156 are open to participants now.

This study's planned enrollment of 134 is above the median of 100 across 367 observational studies indexed under Acute Lung Injury.

Browse Acute Lung Injury studies →

Lead sponsor

Dr Abdurrahman Yurtaslan Ankara Oncology Training and Research Hospital is the lead sponsor of 73 studies on the registry; 19 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years to 85 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

The study population will consist of adult patients aged 18 to 85 years who are scheduled to undergo thoracic surgery at Etlik City Hospital and require OLV during the procedure. Patients will be included if they meet the eligibility criteria of being over 18 years old, undergoing thoracic surgery, receiving intraoperative OLV, and providing informed consent to participate in the study. Patients will be excluded if they are part of the pediatric age group, do not require OLV, or decline participation. A total of 134 eligible patients will be prospectively enrolled and followed for seven days postoperatively to assess the occurrence of pulmonary complications.

Inclusion criteria

Age ≥18 years Undergoing thoracic surgery OLV planned during the procedure

Exclusion criteria

Exclusion Criteria:

Pediatric patients Patients not requiring OLV Previous thoracic surgery

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Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
134 participants (estimated)
Patient registry
No

Interventions

  • ProcedureOne-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.

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What researchers measure

Primary outcomes

  1. Postopertive Pulmonary Complications

    Postoperative pulmonary complications (PPCs) are defined as respiratory events occurring within the first seven days following thoracic surgery, which negatively impact patient outcomes. In this study, PPCs include pneumonia, pneumothorax, hemothorax, acute lung injury, acute respiratory distress syndrome (ARDS), prolonged oxygen requirement, unplanned reintubation, and the need for non-invasive ventilation. These complications will be identified through clinical assessment, arterial blood gas analysis, and postoperative imaging such as chest X-rays. Each case will be evaluated using predefined diagnostic criteria to ensure consistency. The incidence of PPCs will be analyzed in relation to the duration of intraoperative single-lung ventilation.

    Time frame: postoperative 7 days

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Study locations

1 of 1 sites recruiting
  • Hazal Ekin GÜRAN AYTUĞ
    Ankara, Ankara 06810, Turkey (Türkiye)
    Recruiting
08

References and documents

Publications

  • Miskovic A, Lumb AB. Postoperative pulmonary complications. Br J Anaesth. 2017 Mar 1;118(3):317-334. doi: 10.1093/bja/aex002. PubMed 28186222 ↗
  • Kiss T, Bluth T, Gama de Abreu M. [Does intraoperative lung-protective ventilation reduce postoperative pulmonary complications?]. Anaesthesist. 2016 Aug;65(8):573-9. doi: 10.1007/s00101-016-0198-8. German. PubMed 27392439 ↗

Individual participant data

Plan to share: No

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Dec 18, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT07100860
Lead sponsor
Dr Abdurrahman Yurtaslan Ankara Oncology Training and Research Hospital
Responsible party
Ekin Guran, MD (Consultant Anesthesiologist, Ankara Etlik City Hospital) — Principal investigator
First posted
Aug 3, 2025
Start date
Jan 1, 2025
Primary completion
Dec 1, 2025
Completion
Jan 1, 2026 (estimated)
Last update
Dec 18, 2025

Study contacts

Hazal EG AYTUĞ
Contact
drekinguran@gmail.com
05078448449
Hazal EG AYTUĞ
study director · Consultant Anesthesiologist

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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