- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01627470
Comparison of Continuous Non-invasive Pressure Device Versus Invasive Pressure Measurement During Prehospital Emergency
Evaluation of a Continuous Non-invasive Arterial Pressure Device in Comparison With Invasive Pressure Measurement During Out-of-hospital Emergency
The aim of the study is to evaluate the accuracy of continuous non-invasive AP monitoring (CNAP) compared to simultaneous IBP measurement in intensive care patients undergoing a transport in the ambulance car.
Since CNAP finger blood pressure is calibrated to NBP level, a systematic bias between IBP and CNAP as described by a recent FDA meta analysis [ ] is expected. The most important factor of CNAP system performance is its ability to accurately track blood pressure changes. Thus, the purpose of this investigation is to show that the bias between CNAP and IBP falls within the expected range and that blood pressure alterations are detected instantaneously.
The endpoints of the study are:
- The agreement of systolic, diastolic and mean CNAP and IBP readings determined on a beat-to-beat basis during:
- Takeover of the patient on the intensive care unit,
- Transport of the patient from the intensive care unit to the ambulance car
- Transport of the patient in the ambulance car
- The agreement of systolic, diastolic and mean CNAP and IBP blood pres-sure changes determined on a beat-to-beat basis during:
- Takeover of the patient on the intensive care unit,
- Transport of the patient from the intensive care unit to the ambulance car
- Transport of the patient in the ambulance car
The beat-to-beat readings of CNAP and IBP will be automatically recorded electronically on a memory card in the transport monitor. CNAP data will additionally be recorded directly on the CNAP Monitor with a memory stick. Safety will be assessed by clinical observations as well as adverse events (AE) recording.
Study Overview
Detailed Description
Study Type
Enrollment (Anticipated)
Contacts and Locations
Study Locations
-
-
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Kiel, Germany, 24105
- Recruiting
- University Hospital Schleswig-Holstein - Campus Kiel
-
Contact:
- Florian Reifferscheid, Dr. med.
- Phone Number: +49 431 597 2991
- Email: reifferscheid@uksh.de
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- Patients willing and capable of giving informed consent or with legal agents willing of giving informed consent
- Patients undergoing a transport from the intensive care unit to another institution with the ambulance car
- Patients where the IBP cannula was already placed on the intensive care unit
- Patients where IBP cannula, and CNAP upper arm cuff can be placed on the same arm, and CNAP finger cuff can be placed on the contra-lateral arm
- Intact perfusion of both arm evidenced by a negative Allen's test
- Age 18 years and above
- ASA I-IV
- Weight >= 40 and <= 180 kg, BMI < 35
Exclusion Criteria:
- Patients with history of neurological, neuromuscular seizure
- Patients where IBP cannula cannot be placed in the radial artery
- Patients with vascular implants at the sites of non-invasive blood pressure measurement (fingers and upper arm)
- Patients with history of arrhythmias
- Edematous patients
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Cohort
Emergency Patients with applied arterial blood pressure measurement
|
Continuous non-invasive arterial blood pressure recording
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
agreement with invasive blood pressure
Time Frame: 1 year
|
beat-to-beat readings of CNAP and IBP
|
1 year
|
Collaborators and Investigators
Sponsor
Investigators
- Study Chair: Robert Hanss, PD Dr., UKSH-Campus Kiel
Study record dates
Study Major Dates
Study Start
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- CNAP-ITW
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.
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