- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07237347
Perceptions and Ultrasound Literacy for Sound Volume Management (PULSE)
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
This multicenter survey study aims to explore the experiences, perceptions, and attitudes of intensive care unit (ICU) physicians in Switzerland regarding the use of ultrasound for fluid management. The primary objective is to assess participants' knowledge of ultrasound techniques to predict fluid responsiveness and evaluate venous congestion. The study will also compare familiarity with traditional methods (e.g., central venous pressure, IVC-Inferior Vena Cava ultrasound) and newer approaches such as the VEXUS (Venous Excess Ultrasound Score) score or assessment of stroke volume changes during passive leg raise or mini fluid challenges.
Participants will complete an online questionnaire via REDCap, covering demographics, professional background, ultrasound training, knowledge and experience with ultrasound for volume management and venous congestion, as well as institutional factors and suggestions for improvement. The survey will be distributed to physicians working in ICUs at multiple Swiss hospitals, including the University Hospital Basel, Kantonsspital Aarau, Inselspital Bern, Spitalzentrum Biel, and Triemlispital Zürich. Participation is voluntary, and informed consent will be obtained electronically at the start of the questionnaire.
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Contact
- Name: Gregor Loosen, MD
- Phone Number: +41 61 55 65194
- Email: gregormichael.loosen@usb.ch
Study Contact Backup
- Name: Sebastian Berger, MD
- Phone Number: +41 61 32 84085
- Email: sebastian.berger@usb.ch
Study Locations
-
-
-
Basel, Switzerland, 4031
- University Hospital Basel
-
Contact:
- Gregor Loosen, MD
- Phone Number: +41 61 55 65194
- Email: gregormichael.loosen@usb.ch
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- physicians working in ICUs
- working in Switzerland
Exclusion Criteria:
-
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
ICU staff
physicians working in ICUs in Switzerland
|
physicians working in ICUs will complete a questionnaire through REDcap
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Physician Knowledge and Experience Using Ultrasound for Fluid Management and Venous Congestion
Time Frame: completion of questionnaire takes about 30 minutes
|
The primary outcome is the proportion of ICU physicians in Switzerland who demonstrate knowledge and report regular use of ultrasound techniques for assessing fluid responsiveness and venous congestion, including traditional methods and newer approaches.
Data will be collected through a structured online questionnaire.
|
completion of questionnaire takes about 30 minutes
|
Collaborators and Investigators
Investigators
- Principal Investigator: Gregor Loosen, MD, University Hospital of Basel
Study record dates
Study Major Dates
Study Start (Estimated)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- am25Loosen;Req-2025-00684
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
Clinical Trials on Volume Responsiveness
-
Technical University of MunichUnknownPrediction of Volume ResponsivenessGermany
-
St. Boniface HospitalWithdrawn
-
Universitätsklinikum Hamburg-EppendorfOregon Health and Science University; CSEM Centre Suisse d'Electronique et...WithdrawnComparison of Availability for Prediction of Volume Responsiveness | Comparison of Limits of Agreement for Invasive and Non-invasive Measurement of Stroke Volume VariationGermany
-
Tanta UniversityCompletedSepsis | Fluid Responsiveness | Transthoracic Echocardiography | Electrical Cardiometry | Stoke VolumeEgypt
-
University Hospital, BordeauxCompletedFluid Responsiveness | Volume ExpansionFrance
-
Charles University, Czech RepublicUnknownSeptic Shock | Vein Collapsibility | Intravascular Doppler | Volume Responsiveness in Septic ShockCzechia
-
CHU de ReimsCompletedFluid Responsiveness | Preload ResponsivenessFrance
-
Chinese PLA General HospitalUnknownFluid Therapy | Fluid Responsiveness | Stroke Volume Variation | Pulse Pressure VariationChina
-
RenJi HospitalNot yet recruitingFluid Responsiveness | Stroke Volume Variation | SVV-FloTrac | Thoracic Electrical BioimpedanceChina
-
RenJi HospitalNot yet recruitingFluid Responsiveness | Stroke Volume Variation | SVV-FloTrac | Thoracic Electrical BioimpedanceChina