Passive Leg Raise During Cardiopulmonary Resuscitation

Hemodynamic Instability Clinical Trial

Official title:

Impact of Passive Leg Raise on Hemodynamic Effect: A Randomized Crossover Experimental Study

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT03617978
• Other study ID #: PLR_2018_UL
• Status: Recruiting
• Phase: N/A
• Start date: August 1, 2018
• Est. completion date: September 2018

Study information

• Verified date: August 2018
• Source: Lazarski University
• Contact: Lukasz Szarpak, PhD
• Phone: 500186225
• Email: lukasz.szarpak[@]gmail.com
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

during cardiopulmonary resuscitation, an important element of the procedure is to achieve optimal organ perfusion. For this purpose, high quality chest compressions is one of the basic elements of the procedure. however, similarly as in the case of hypovolemic shock, elevation of the lower limbs may be helpful. The study is a randomized cross-over study and includes the effect of lower limb elevation on hemodynamic parameters in healthy participants.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 110
• Est. completion date: September 2018
• Est. primary completion date: September 2018
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• healthy participants

• voluntary informed consent

Exclusion Criteria:

• hip injury during the six months preceding the examination

• back pain

• kidney damage

Related Conditions & MeSH terms

• Cardiopulmonary Resuscitation
• Hemodynamic Instability
• Leg Elevation

Intervention

Procedure:
• Hemodynamics parameters
real-time evaluation of cardiac output parameters using the ICON device

Locations

Country	Name	City	State
Poland	Faculty of Medicine, Lazarski University	Warsaw	Masovian

Sponsors (2)

Lead Sponsor	Collaborator
Lazarski University	Wroclaw Medical University

Country where clinical trial is conducted

Poland, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Cardiac output - CO	the volume of blood that the heart pumps into blood vessels in one minute. It is the product of the frequency of heart contractions (HR) and stroke volume (SV). The parameter is measured using ICON device	during procedure
Secondary	Stroke Volume - SV	the amount of blood pressed through one of the heart chambers into the appropriate arterial reservoir during a single heart contraction. The parameter is measured using ICON device	during procedure
Secondary	thoracic fluid content - TFC	It is an indicator of total fluid volume, both intracellular and extracellular. The parameter is measured using ICON device	during procedure