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.
UNKNOWN
NA
110 participants
INTERVENTIONAL
2018-08-01
2018-09-30
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Passive Leg Raise (PLR) During Cardiopulmonary Resuscitation (CPR)
NCT01952197
Hemodynamic Variations During Remote Ischemic Conditioning in Critical Ill Patients
NCT06536231
Influence of Posture and Positioning in Rescuer's Fatigue and Quality of Chest Compressions
NCT05405569
Effectiveness of Chest Compressions Under Mild Hypoxia
NCT04072484
Plasma Biomarkers and Platelet Morphology of Extracorporeal CardioPulmonary Resuscitation
NCT07113769
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.
RANDOMIZED
CROSSOVER
TREATMENT
SINGLE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
None Elevation
Participant placed on a flat surface. Study participant connected to the measuring hemodynamic parameters device
Hemodynamics parameters
real-time evaluation of cardiac output parameters using the ICON device
Elevation angle of 20 degrees
Participant placed on a flat surface, lower limbs raised and supported at an angle of 20 degrees. Study participant connected to the measuring hemodynamic parameters device
Hemodynamics parameters
real-time evaluation of cardiac output parameters using the ICON device
Elevation angle of 30 degrees
Participant placed on a flat surface, lower limbs raised and supported at an angle of 30 degrees. Study participant connected to the measuring hemodynamic parameters device
Hemodynamics parameters
real-time evaluation of cardiac output parameters using the ICON device
Elevation angle of 45 degrees
Participant placed on a flat surface, lower limbs raised and supported at an angle of 45 degrees. Study participant connected to the measuring hemodynamic parameters device
Hemodynamics parameters
real-time evaluation of cardiac output parameters using the ICON device
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Hemodynamics parameters
real-time evaluation of cardiac output parameters using the ICON device
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* voluntary informed consent
Exclusion Criteria
* back pain
* kidney damage
18 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Wroclaw Medical University
OTHER
Lazarski University
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Łukasz Szarpak
Associate Professor
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Faculty of Medicine, Lazarski University
Warsaw, Masovian Voivodeship, Poland
Countries
Review the countries where the study has at least one active or historical site.
Central Contacts
Reach out to these primary contacts for questions about participation or study logistics.
Facility Contacts
Find local site contact details for specific facilities participating in the trial.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
PLR_2018_UL
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.