Do you think you're having difficulty controlling your high blood pressure?
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- STATUS
- Recruiting
Summary
Do you think you're having difficulty controlling your high blood pressure?
Description
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
Details
| Condition | High Blood Pressure (Hypertension) |
|---|---|
| Clinical Study Identifier | TX136186 |
| Last Modified on | 8 November 2020 |
Eligibility
How to participate?
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Your message has been sent to the study team at ,
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.
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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.
Learn moreIf 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 moreComplete 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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