Men and Women ages 18 or older with High Blood Pressure and Diabetes Type 2 who DO NOT require the use of Insulin to control their Diabetes Levels

  • STATUS
    Recruiting
Updated on 8 November 2020

Summary

Men and Women ages 18 or older with High Blood Pressure and Diabetes Type 2 who DO NOT require the use of Insulin to control their Diabetes Levels

Description

A 8 to 12 Week Randomized, Double-Blind Study to Compare the Fixed-Dose Combination of Telmisartan 80 + Amlodipine 10mg Versus Amlodipine 10mg Monotherapy as First Line Therapy in Type 2 Diebetes Patients with Hypertension (High Blood Pressure)

Patient Inclusion Criteria:

  • Men or Women
  • 18 Years of Age or Older
  • May consent to study in English/Spanish: read, write & understand
  • Diagnosis of Diabetes Type 2
  • Diagnosis of High Blood Pressure
  • Comply all study visits required

Patient Exclusion Criteria:

  • Insulin Use to Control Diabetes Type 2
  • Unable to understand study Informed Consent Form and other Instructions given in study
  • Unwilling to comply with all study visits required
  • Night Shift Time Worker (requires sleep time to be during the day)

Details
Condition Diabetes and Hypertension, Cardiovascular Abnormalities, High Blood Pressure (Hypertension), Heart Disease, Vascular Diseases
Clinical Study IdentifierTX134660
Last Modified on8 November 2020

Eligibility

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.

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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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