Non-Dipping Hypertension and The Human Chronobiome | Clinical Research Studies Listing

Recruiting

18 years - 99 years

All

Phase 1

150 participants needed

1 Location

Brief description of study

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.

Detailed description of study

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.

Eligibility of study

You may be eligible for this study if you meet the following criteria:

Conditions: Hypertension, blood pressure
Age: 18 years - 99 years
Gender: All

Updated on 19 Feb 2024. Study ID: 828944

Find a site

Your Information has been sent successfully.

Message sent successfully.

We have submitted the information you provided to the research team at the location you chose. For your records, we have sent a copy of the message to your email address.

If you would like to be informed of other studies that may be of interest to you, you may sign up for Patient Notification Service.

Send a message

Enter your contact details to connect with study team

First name*

Last name*

Email*

Phone number*

Preferred way of contact

Race

Ethnicity

Are you Healthy Volunteer

Other language

By sending a message, I agree that my data will be sent to a representative for the selected site and processed in accordance with this website's Privacy Policy (see link in footer).