Prediction of Fluid Responsiveness From Passive Leg Raising Induced Changes in Perfusion Index and Pleth Variability Index
NCT ID: NCT03499860
Last Updated: 2019-07-22
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.
COMPLETED
NA
51 participants
INTERVENTIONAL
2018-04-20
2019-04-01
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Fluid responsive patients are defined as showing an increase in cardiac output \>10% during a passive leg raising test, measured semi-invaseively with FloTracĀ® (Edwards LifeSciences. Irvine, United States).
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Peripheral Venous Pressure Variation and Fluid Responsiveness
NCT05131516
Arterial Pressure Derived Dynamic Parameters to Detect Preload Responsiveness in Spontaneously Breathing Patients
NCT06480942
Assessment of Fluid Responsiveness by Elevation of PEEP in Patients With Septic Shock
NCT01827007
Clinical Validation of Algorithms for Mean Systemic Filling Pressure and Automated Cardiac Output
NCT04202432
Impact of Fluid Resuscitation Therapy on Pulmonary Edema as Measured by Alveolar Fluid Clearance in Patients With Acute Respiratory Distress Syndrome (ARDS)
NCT01763853
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
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.
NA
SINGLE_GROUP
DIAGNOSTIC
NONE
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Passive Leg Raising Test
A passive leg raising test is performed in all patients included in the study
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Spontaneous breathing
* Arterial line already in place
* Oral and written informed consent obtained
Exclusion Criteria
* Abdominal trauma as the reason for surgery
* Missing informed consent
18 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Department of Anaesthesiology, Merano Hospital, Italy
UNKNOWN
Institute of Mountain Emergency Medicine
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Simon Rauch
Researcher
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
"F. Tappeiner" Hospital Merano
Merano, Bolzano, Italy
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
06
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.