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Passive Leg Raising - an Important Diagnostic Manoeuvre (PLR-ANS)

R

Region MidtJylland Denmark

Status

Completed

Conditions

Cardiovascular Insufficiency

Treatments

Diagnostic Test: Passive Leg Raising

Study type

Interventional

Funder types

Other
Industry

Identifiers

Details and patient eligibility

About

The aim is to describe the physiological background for PLR and the interpretation of a PLR manoeuvre.

The protocol entails the measurement of stroke volume (SV) at baseline (semirecumbent patient position), during PLR and after returning to semirecumbent position. Simultaneously blood pressure (BP), pulse rate (PR), pulse oximetric saturation (SpO2) and ECG are recorded. The procedure is performed in ten normal subjects, ten patients recruited in the cardiology outpatient department and ten critically ill patients under analgosedation in the ICU.

Analysis includes changes in measured variables and heart rate variability in the frequency domain during the three phases of the experiment.

Full description

See above

Enrollment

11 patients

Sex

All

Ages

18 to 80 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

Consenting after written and oral information

Exclusion criteria

Contraindications to PLR: intracranial or abdominal hypertension

Trial design

Primary purpose

Basic Science

Allocation

Non-Randomized

Interventional model

Sequential Assignment

Masking

Single Blind

11 participants in 3 patient groups

Normal subjects
Active Comparator group
Description:
Normal subjects 'Passive Leg Raising'
Treatment:
Diagnostic Test: Passive Leg Raising
ICU patients
Active Comparator group
Description:
ICU patients 'Passive Leg Raising'
Treatment:
Diagnostic Test: Passive Leg Raising
Cardiac Outpatients
Active Comparator group
Description:
Cardiac Outpatients 'Passive Leg Raising'
Treatment:
Diagnostic Test: Passive Leg Raising

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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