Decremental Esophageal Catheter Filling Volume Titration For Transpulmonary Pressure Measurement
NCT06051292 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 27
Last updated 2025-03-20
Summary
Mechanical ventilation is a critical intervention in the management of pediatric patients with respiratory distress. During this process, accurate measurement of transpulmonary pressure (PL) is essential to ensure the safety and efficacy of ventilation. PL is defined as the difference between alveolar pressure (Palv) and pleural pressure (Ppl). While the direct measurement of Ppl is possible, it poses a risk to tissue integrity. Thus, the primary surrogate for Ppl measurement today is esophageal pressure (Pes).
However, the measurement of Pes is not without challenges. This abstract outlines the pitfalls associated with Pes measurement, emphasizing the importance of employing well-defined procedures to mitigate potential errors. These errors can range from underestimation of Pes due to underfilled catheters to overestimation resulting from overfilled catheters.
To address these challenges and optimize Pes measurement, various methods have been proposed for titrating the filling volume of the esophageal catheter. In this study, investigators aim to assess a faster decremental filling method and compare it to the traditionally accepted Mojoli method in the context of pediatric patients. This research seeks to enhance the intensivists' understanding of the most efficient and accurate approach to Pes measurement during mechanical ventilation in the pediatric population, ultimately contributing to improved patient care and outcomes
Conditions
- Pediatric Acute Respiratory Distress Syndrome (PARDS)
- Acute Respiratory Failure
- Acute Respiratory Distress Syndrome
Interventions
- OTHER
-
Fast method
Fast decremental catheter volume titration will be applied and optimal filling volume will be determined according to the measurements
- OTHER
-
Conventional method
Conventional catheter volume titration will be applied and optimal filling volume will be determined according to the measurements
Sponsors & Collaborators
-
Dr. Behcet Uz Children's Hospital
lead OTHER
Principal Investigators
-
Hasan Agin, Professor · Behcet Uz Children's Hospital
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- DOUBLE
- Model
- CROSSOVER
Eligibility
- Min Age
- 1 Month
- Max Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2023-09-18
- Primary Completion
- 2025-11-30
- Completion
- 2025-12-30
Countries
- Turkey (Türkiye)
Study Locations
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