Non-Dipping Hypertension and The Human Chronobiome

  • STATUS
    Recruiting
  • participants needed
    150
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Updated on 19 February 2024

Summary

The NDHTEN-Chronobiome study team will receive a request to deploy a 24h-ABPM. The study doctor's will make the results from the ambulatory blood pressure monitor (APBM) available to your physician. Measuring your blood pressure over the course of 24 hours will identify whether your blood pressure is lowering at night compared to your blood pressure readings during the day.

Description

The study will consist of two visits to the Hospital of the University of Pennsylvania (HUP). Two devices will be applied for 24 hours. The 1st device is called the ambulatory blood pressure monitor (APRM) and the 2nd device is the actigraph activity recorder that is placed on your wrist area. Those who do not have lower blood pressure at night may be invited to participate in Part 1 of this study which includes a separate consent form.

FAQ


Details
Condition Hypertension, blood pressure
Age 18years - 99years
Clinical Study Identifier03598894
Last Modified on19 February 2024

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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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