Actively Recruiting
Assessment of the Effects of Prone Positioning on Ventilation Homogenization in ARDS Patients by the Phase III Slope of the Volumetric Capnography
Led by Istanbul University - Cerrahpasa · Updated on 2024-07-03
60
Participants Needed
1
Research Sites
4 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are evaluating the effects of prone positioning on improving ventilation distribution in patients with Acute Respiratory Distress Syndrome (ARDS) who are intubated and mechanically ventilated due to respiratory failure. This observational study focuses on understanding how turning patients onto their stomachs affects lung function, particularly looking at the slope of the volumetric capnography phase III, which relates to ventilation homogenization. The study is sponsored by Istanbul University - Cerrahpasa and involves standard care procedures for ARDS patients. Participants will undergo prone positioning, where they are turned onto their stomachs and remain in this position for at least 16 hours and up to 24 hours, following ARDS guidelines. Before and after this intervention, measurements including low-flow pressure volume curves, airway opening pressure, and recruitment-to-inflation ratios will be assessed to optimize positive end-expiratory pressure. The phase III slope of the volumetric capnograph will be recorded at four time points: before prone positioning, immediately after, at the end of the prone cycle, and after returning to the supine position. During the study, patients will be closely monitored with several lung function assessments, including correlation measures between the phase III slope and oxygenation indices like PaO2/FiO2 ratio. Data collection will occur at specific intervals aligned with the prone positioning duration. The primary outcome centers on changes in the phase III slope after prone positioning. The study period extends up to 24 hours of prone positioning with ongoing observations to understand ventilation improvements in severe ARDS cases.
CONDITIONS
Brief Title
Change in the Phase III Slope of the Volumetric Capnography by Prone Positioning in Acute Respiratory Distress Syndrome
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Meets criteria for Acute Respiratory Distress Syndrome (ARDS)
- Intubated and mechanically ventilated due to respiratory failure
- PaO2/FiO2 ratio less than 200
- Age 18 years or older
You will not qualify if you...
- Chronic pulmonary disease
- Presence of pneumothorax
- Intraabdominal hypertension greater than 12 mmHg
- Pregnancy
- Not expected to survive more than 24 hours
- Hemodynamic instability
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - 16 to 24 hours
Participants who are intubated and mechanically ventilated undergo standard assessments and measurements as part of routine care, including recording the phase III slope of the volumetric capnography at specified timepoints related to prone positioning.
4 measurement timepoints during a single prone positioning cycle
Trial Site Locations
Total: 1 location
1
Hamidiye Etfal Hospital
Istanbul, Turkey (Türkiye), 34000
Actively Recruiting
Research Team
O
Olcay Dilken, MD
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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