Do you think you're having difficulty controlling your high blood pressure?

Updated on 8 November 2020


Do you think you're having difficulty controlling your high blood pressure?


Many people struggle to control their high blood pressure, a disease known as hypertension. New medical treatments can be a way to make high blood pressure easier to control. Medical research works towards finding those new treatments.

You will be taking a combination of study medications or a single type of study medication. If you need adjustments to your current medications, your study doctor wil adjust your medicines accordingly.

When you take part in this clinical research study:

  • Study health professionals monitor your hypertension and blood pressure.
  • Qualified participants will receive: study medication at no cost, study-related medical care (such as exams and lab tests) at no cost, possible compensation for time and travel.

Patient Inclusion Criteria

  • Are at least 18 years old
  • Have been diagnosed with hypertension (high blood pressure)
  • Are not pregnant, or not planning to become pregnant
  • Do not have Type 1 diabetes

Patient Exclusion Criteria

  • Secondary hypertension or severe hypertension
  • Clinically significant cardiovascular disease or heart failure
  • Clinical significant respiratory disease that would prohibit the use of a beta blocker
  • A medical contraindication to discontinuing a current antihypertensive therapy
  • History of Type 1 diabetes mellitus
  • History of Severe Mental Illness except mild depression

Condition High Blood Pressure (Hypertension)
Clinical Study IdentifierTX136186
Last Modified on8 November 2020


How to participate?

Step 1 Connect with a study center
What happens next?
  • You can expect the study team to contact you via email or phone in the next few days.
  • Sign up as volunteer  to help accelerate the development of new treatments and to get notified about similar trials.

You are contacting

Investigator Avatar

Primary Contact


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

Learn more

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.

Learn more

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

Learn more

Similar trials to consider


Not finding what you're looking for?

Every year hundreds of thousands of volunteers step forward to participate in research. Sign up as a volunteer and receive email notifications when clinical trials are posted in the medical category of interest to you.

Sign up as volunteer

user name

Added by • 



Reply by • Private

Lorem ipsum dolor sit amet consectetur, adipisicing elit. Ipsa vel nobis alias. Quae eveniet velit voluptate quo doloribus maxime et dicta in sequi, corporis quod. Ea, dolor eius? Dolore, vel!

  The passcode will expire in None.

No annotations made yet

Add a private note
  • abc Select a piece of text from the left.
  • Add notes visible only to you.
  • Send it to people through a passcode protected link.
Add a private note