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Study of Co-administration of Olmesartan Medoxomil Plus Amlodipine in Patients With Mild to Severe Hypertension

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Daiichi Sankyo

Status and phase

Completed
Phase 3

Conditions

Hypertension

Treatments

Drug: Olmesartan medoxomil
Drug: Amlodipine

Study type

Interventional

Funder types

Industry

Identifiers

NCT00185133
CS8663-A-U301

Details and patient eligibility

About

This study assesses the efficacy and safety of co-administration of olmesartan medoxomil plus amlodipine in mild to severe hypertensive patients older than 18 years of age

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Male or female patients
  • 18 years of age or older (20% equal to or older than 65 years)
  • With mild to severe hypertension defined as seated diastolic blood pressure of 95-120 mmHg while off any hypertensive medication

Exclusion criteria

  • Patients should not have serious concomitant conditions that could interfere with the analysis of the results or that could interfere with the well-being of the patients

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

Trial contacts and locations

139

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Data sourced from clinicaltrials.gov

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