Enrolling study
Research Study in Adults With High Blood Pressure
A cardiovascular research study for adults whose blood pressure remains above goal despite current therapy.
About this study
The study team collects blood pressure readings, laboratory results, and safety information while participants take either the investigational medication or a comparator, as described in the informed consent document.
- Condition
- High Blood Pressure
- Age range
- 21–80
- Estimated duration
- About 9 months
- Study visits
- 7
Eligibility snapshot
- Adults 21–80 years of age
- Documented history of high blood pressure
- Blood pressure above goal at screening
- Willing to complete home blood pressure readings
What to expect
- 1Screening visit with informed consent review
- 2Approximately 7 in-clinic visits
- 3Electrocardiograms and routine laboratory testing
- 4Home blood pressure log kept between visits
Compensation
Compensation for time and travel may be available.
Location & Principal Investigator
8500 Example Medical Plaza, Suite 210, Miami, FL 33176
Studies at this site are conducted by our Principal Investigators and research staff.
Frequently asked questions
Answers to questions we hear most often.
What does participation involve?
Participation involves scheduled study visits with assessments defined by the protocol. Everything that will be asked of you is described in the informed consent document before you decide.
How long is the study?
The estimated duration is listed above. Your coordinator will review the full visit schedule with you during the consent process.
Will I be compensated for time and travel?
Where compensation is offered, the amount and payment schedule are described in the informed consent document and reviewed with you before enrollment.
What are the eligibility requirements?
The listing above shows a high-level snapshot. Full criteria are defined in the protocol and confirmed by the study team at a screening visit.
Can I leave the study at any time?
Yes. Participation is voluntary and you may withdraw at any time. Your coordinator will discuss any recommended safety follow-up.
Is my information kept confidential?
Yes. Access is limited to delegated study staff, and information shared with the sponsor is coded wherever the protocol allows.
Think you may qualify?
Contact us to learn more. A short conversation is all it takes to find out whether a screening visit makes sense.
Contact us to pre-screenThis study is conducted under IRB oversight in accordance with Good Clinical Practice guidelines. Eligibility is confirmed by the study team; the information here is a summary and not a full protocol.