Phase 2 Study to Evaluate the Efficacy and Safety of Irbesartan and Amlodipine Combined or Alone in Patients With Essential Hypetension

  • STATUS
    Recruiting
  • participants needed
    440
  • sponsor
    Handok Inc.
Updated on 19 February 2024
hypertension
essential hypertension
amlodipine
irbesartan

Summary

A Randomized, Double-blind, Multicenter, Factorial Design, Phase II Study to Evaluate the Efficacy and Safety of Irbesartan and Amlodipine Combined or Alone in Patients With Essential Hypertension

Details
Condition Essential Hypertension
Age 19years - 75years
Treatment Irbesartan/Amlodipine
Clinical Study IdentifierNCT04488978
SponsorHandok Inc.
Last Modified on19 February 2024

Eligibility

Yes No Not Sure

Inclusion Criteria

Patients who are 19 years or older / 75 years or younger on screening
Signed informed consent
Patients with Essential Hypertension
Other inclusion applied

Exclusion Criteria

Orthostatic hypertension with symptom
Other exclusion applied
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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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