Trial document





This trial has been registered retrospectively.
drksid header

  DRKS00011288

Trial Description

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Title

Characterization of the patient collective of the University Center of Hypertension Colone in a registry

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Trial Acronym

[---]*

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URL of the Trial

http:///

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Brief Summary in Lay Language

[---]*

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Brief Summary in Scientific Language

This research project introduces a registry for patients with actual or suspected resistant hypertension. All data of patients being treated in the clinical routine in the University Center of Hypertension Cologne according to the latest guidelines are documentated and analyzed. We aim to establish a better understanding of resistant hypertension, its prevalence, ris factors, sequelaes and consequences. This may lead to better and individual therapy strategy for the patient.
Being aware of the high prevalence of non-compliance in hypertensive patients we established a routine method for measuring the level of antiyhpertensive medication in blood samples. With this tool the identification of actual resistand hypertension is simplified.
Besides the compliance it is important to rule out secondary causes of hypertension to identify resistant hypertension.
With the given data analyzed we hope to improve the managment and therapy of patients with resistant hypertension, which may lead to a lower cardiovascular risk in individual patients.
The University Center of Hypertension Cologne is suitable for this project because of the high prevalence of patients being diagnosed with resistant hypertension in our collective.

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Organizational Data

  •   DRKS00011288
  •   2017/01/13
  •   [---]*
  •   yes
  •   Approved
  •   16-402, Ethik-Kommission der Medizinischen Fakultät der Universität zu Köln
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Secondary IDs

  • [---]*
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Health Condition or Problem studied

  •   I10.01 -  [generalization I10: Essential (primary) hypertension]
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Interventions/Observational Groups

  •   Data being assessed in clinical routine of patients being diagnosed with resistant hypertension are anonymously documentated and analyzed. There is only one observational arm.
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Characteristics

  •   Non-interventional
  •   Observational study
  •   Single arm study
  •   Open (masking not used)
  •   [---]*
  •   Uncontrolled/Single arm
  •   Other
  •   Single (group)
  •   N/A
  •   N/A
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Primary Outcome

There are no primary endpoints. All data of the clinical routine are documentated in a registry for later observational analysis

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Secondary Outcome

/

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Countries of Recruitment

  •   Germany
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Locations of Recruitment

  • University Medical Center 
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Recruitment

  •   Actual
  •   2016/11/03
  •   1000
  •   Monocenter trial
  •   National
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Inclusion Criteria

  •   Both, male and female
  •   18   Years
  •   no maximum age
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Additional Inclusion Criteria

All patients of the University Center of Hypertension of Cologne, who are diagnosed with resistant hypertension according to the latest guidelines

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Exclusion Criteria

-Patients without the diagnosis auf resistant hypertension
-Age under 18

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Addresses

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    • Medizinische Klinik III, Herzzentrum des Universitätsklinikums Köln, Hypertoniezentrum
    • Mr.  Fabian  Hoffmann 
    • Kerpenerstraße 62
    • 50937  Köln
    • Germany
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    • Medizinische Klinik III, Universitätsklinikum Köln, Hypertoniezentrum
    • Mr.  Fabian  Hoffmann 
    • Kerpenerstraße 62
    • 50937  Köln
    • Germany
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    end of 1:1-Block address contact scientific-contact
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    • Medizinische Klinik III, Universitätsklinikum Köln, Hypertoniezentrum
    • Mr.  Fabian  Hoffmann 
    • Kerpenerstraße 62
    • 50937  Köln
    • Germany
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Sources of Monetary or Material Support

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    • Medizinische Klinik III, Universitätsklinikum Köln, Hypertoniezentrum
    • Mr.  Prof. Dr. med.  Hannes  Reuter 
    • Kerpenerstraße 62
    • 50937  Köln
    • Germany
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Status

  •   Recruiting ongoing
  •   [---]*
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Trial Publications, Results and other Documents

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* This entry means the parameter is not applicable or has not been set.