Transducer Levelling Errors in Everyday ICU Practice - A Multicentre Blinded Observational Study
NCT ID: NCT07330505
Last Updated: 2026-01-09
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
NOT_YET_RECRUITING
60 participants
OBSERVATIONAL
2026-02-01
2027-02-01
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
This prospective, multicenter, blinded observational study will quantify transducer levelling deviations during routine ICU care and evaluate whether clinically relevant deviations are associated with treatment decisions. Adult mechanically ventilated ICU patients with an arterial catheter, a central venous catheter, and ongoing vasopressor therapy will be included at hospitals in Västra Götalandsregionen, Sweden. Two blinded reference lines/sensors will be placed at predefined physiological zero levels for MAP and CVP and connected in parallel to the patient monitoring system. Continuous deviation (mmHg) between the clinical transducer position and the blinded reference level will be recorded for 8 hours while clinical staff remain unaware of the reference setup. MAP/CVP-related treatment decisions (e.g., vasopressor adjustments, fluid therapy, and nursing interventions) will be recorded with timestamps.
The study will provide real-world data on the magnitude and frequency of invasive pressure transducer misalignment in daily ICU practice and its potential relationship to patient management.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Reliability of PVI Changes During Tidal Volume Challenge in ICU Patients
NCT05428423
Effectiveness of Goal-Directed Fluid Therapy Guided by Cardiac Index Versus Central Venous Pressure in Major Abdominal Surgery Patients in the ICU.
NCT07303855
NT-proBNP in ICU Postoperative/Posttraumatic Patients With Shock
NCT00736723
Prevalence of Hypotension Associated With Preload Dependence During Continuous Renal Replacement Therapy
NCT03139123
Preload Dependence During Prone Position In ARDS Patients
NCT01965574
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
To quantify levelling deviations without influencing clinical behavior, a parallel reference measurement setup is connected to the existing monitoring system. Two fluid-filled reference lines are connected in parallel to the pressure dome used for invasive monitoring and secured to the chest wall at the fourth intercostal space at half of the anteroposterior thoracic diameter, one on each side of the chest. This configuration allows continuous estimation of vertical deviation (mmHg) between the clinical transducer position and a predefined physiological reference level. During lateral positioning, deviation is calculated using the midpoint between the two reference lines as the reference. Reference lines are covered with dressings to maintain blinding of clinical staff to the reference levels.
Physiological waveforms and calculated deviations are recorded continuously for an 8-hour monitoring period for each participant. In parallel, treatment actions plausibly influenced by interpretation of MAP or CVP (including vasopressor titration, fluid administration or removal, and nursing interventions related to positioning or transducer handling) are documented with timestamps to allow temporal association analyses. Relevant contextual variables are collected to support interpretation of deviations and clinical responses.
Data quality is ensured through predefined measurement procedures, continuous digital waveform acquisition, synchronization of reference and clinical signals, and post hoc review of signal integrity. Periods affected by technical artifacts or signal loss are flagged according to predefined criteria. Data segments that are missing, uninterpretable, or invalid due to technical failure are treated as missing and excluded from analyses, without imputation.
The study is designed to quantify the magnitude and frequency of invasive pressure transducer misalignment during routine ICU care and to explore whether clinically relevant deviations are associated with contemporaneous treatment decisions, with the aim of informing patient safety and quality improvement initiatives.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
COHORT
PROSPECTIVE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Invasive Pressure Monitoring Cohort
Mechanically ventilated adult ICU patients undergoing routine invasive arterial blood pressure and central venous pressure monitoring. Pressure transducer positioning and associated pressure deviations are observed using blinded reference sensors without altering clinical care.
No interventions assigned to this group
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* ICU admission
* Mechanically ventilated
* Arterial catheter for MAP
* Central venous catheter for CVP
* Ongoing vasopressor therapy
Exclusion Criteria
* Contraindications for lateral positioning
* Expected survival \<24 hours
18 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Vastra Gotaland Region
OTHER_GOV
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Carl Sjödin
Principal Investigator
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Lotta Johansson, PhD
Role: PRINCIPAL_INVESTIGATOR
Sahlgrenska University Hospital
Central Contacts
Reach out to these primary contacts for questions about participation or study logistics.
References
Explore related publications, articles, or registry entries linked to this study.
1. Cecconi, M., et al., Consensus on circulatory shock and hemodynamic monitoring. Task force of the European Society of Intensive Care Medicine. Intensive Care Med, 2014. 40(12): p. 1795-815. 2. Vincent, J.L., Critical care - where have we been and where are we going? New England Journal of Medicine, 2013. 369(19): p. 1839-1841. 3. Vincent, J.L. and D. De Backer, Circulatory shock. New England Journal of Medicine, 2013. 369(18): p. 1726-1734. 4. Giusti, G.D., Critical care nurses' perspectives on cardiac monitoring: barriers and training needs. BMC Nursing, 2024. 23: p. 742. 5. Alastalo, T.T., Critical care nurses' observational skills in detecting early patient deterioration. Intensive and Critical Care Nursing, 2017. 43: p. 97-103. 6. Magder, S., Right Atrial Pressure in the Critically Ill: How to Measure, What Is the Value, What Are the Limitations? Chest, 2017. 151(4): p. 908-916. 7. Sjödin, C., S. Sondergaard, and L. Johansson, Variability in alignment of central venous pressure transducer to physiologic reference point in the intensive care unit-A descriptive and correlational study. Aust Crit Care, 2019. 32(3): p. 213-217. 8. Figg, K.K. and E.C. Nemergut, Error in central venous pressure measurement. Anesth Analg, 2009. 108(4): p. 1209-11. 9. Oh, C., et al., Errors in pressure measurements due to changes in pressure transducer levels during adult cardiac surgery: a prospective observational study. BMC Anesthesiol, 2023. 23(1): p. 8. 10. Jacobs, K., et al., Accuracy of intra-arterial line transducer levelling practice in a general intensive care unit. Aust Crit Care, 2024. 37(1): p. 51-57.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
2024-06578-01
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.