Intraoperative Lung Protective Ventilation in Czech Republic
IOLPVCZ
Overview of Intraoperative Lung Protective Ventilation in Czech Republic
1 other identifier
observational
800
0 countries
N/A
Brief Summary
This questionnaire-based study aims to evaluate the adherence to and current clinical practices regarding intraoperative lung-protective ventilation (IOLPV) among anesthesiologists in the Czech Republic. Despite the established role of IOLPV in reducing postoperative pulmonary complications in selected populations, its routine application during general anesthesia for elective surgeries remains variable. The survey focuses on identifying common ventilation strategies, attitudes toward lung recruitment maneuvers, tidal volume selection, use of PEEP, and awareness of existing recommendations. The results will provide insight into national practice patterns, perceived barriers, and educational needs, helping to inform future guidelines, training initiatives, and efforts to enhance patient safety and postoperative outcomes across Czech anesthesia departments.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Feb 2026
Shorter than P25 for all trials
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
December 2, 2025
CompletedFirst Posted
Study publicly available on registry
December 15, 2025
CompletedStudy Start
First participant enrolled
February 1, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
July 1, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
August 1, 2026
December 15, 2025
December 1, 2025
5 months
December 2, 2025
December 2, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Adherence to IOLPV
Number of respondents that respond that meet IOLPV guidelines
20 days
Eligibility Criteria
Anaesthesiologists in Czech republic
You may qualify if:
- anaesthesiologist practiting in Czech republic
You may not qualify if:
- not lincensed anaesthesiologist
- anaesthesiologist outside Czech republic
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Target Duration
- 20 Days
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- deputy for science and research
Study Record Dates
First Submitted
December 2, 2025
First Posted
December 15, 2025
Study Start
February 1, 2026
Primary Completion (Estimated)
July 1, 2026
Study Completion (Estimated)
August 1, 2026
Last Updated
December 15, 2025
Record last verified: 2025-12
Data Sharing
- IPD Sharing
- Will share
IPD will be shared through research office of the main department of the principal investigator on reasonable request.