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Haemodynamic Feasibility Study of Sensors Within a Tilting Table Examination

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ClinicalTrials.gov Identifier: NCT01831297
Recruitment Status : Completed
First Posted : April 15, 2013
Last Update Posted : November 27, 2013
Sponsor:
Information provided by (Responsible Party):

Study Description
Brief Summary:
This study´s aim is to explore physiological associations concerning pulse wave velocity, heart rate and blood pressure in order to make taking the blood pressure more comfortable.

Condition or disease Intervention/treatment
Syncope Device: measurement of blood pressure

Study Design

Study Type : Observational
Actual Enrollment : 10 participants
Observational Model: Cohort
Time Perspective: Prospective
Study Start Date : August 2012
Primary Completion Date : July 2013
Study Completion Date : July 2013

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Fainting
U.S. FDA Resources

Groups and Cohorts

Group/Cohort Intervention/treatment
syncope Device: measurement of blood pressure
measurement of pulse wave velocity


Outcome Measures

Primary Outcome Measures :
  1. data about possible correlation [ Time Frame: 45 minutes ]
    Correlation between pulse wave velocity, pulse rate and blood pressure


Eligibility Criteria

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years to 90 Years   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population
patients with syncope
Criteria

Inclusion Criteria:

  • patients with syncope and planned tilting table investigation
  • male and female patients aged at least 18 years
  • persons being able to understand and to follow the study stuff´s instructions

Exclusion Criteria:

  • pregnancy or breast feeding
  • patients not being able to consent
  • cardiac pacemaker / defibrillator
  • illness of skin
Contacts and Locations

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01831297


Locations
Germany
Univeristy Hospital Aachen
Aachen, North Rhine Westfalia, Germany, 52074
Sponsors and Collaborators
RWTH Aachen University
More Information

Responsible Party: RWTH Aachen University
ClinicalTrials.gov Identifier: NCT01831297     History of Changes
Other Study ID Numbers: 10-082
First Posted: April 15, 2013    Key Record Dates
Last Update Posted: November 27, 2013
Last Verified: November 2013

Additional relevant MeSH terms:
Syncope
Unconsciousness
Consciousness Disorders
Neurobehavioral Manifestations
Neurologic Manifestations
Nervous System Diseases
Signs and Symptoms