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Safety and Efficacy of Ramipril in the Treatment of Essential Hypertension

P

Pacific Pharmaceuticals

Status and phase

Unknown
Phase 4

Conditions

Essential Hypertension

Treatments

Drug: Ramipril

Study type

Interventional

Funder types

Industry

Identifiers

NCT00366119
RMN-P01

Details and patient eligibility

About

The purpose of this study is to assess which drug is more effective of Ramiprin®(ramipril) and Tritace®(ramipril) in the Treatment of Essential Hypertension

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • mild and moderate essential hypertension (90mmHg≤DBP≤110mmHg)

Exclusion criteria

  • 180mmHg≤SBP
  • If differences greater than 20mmHg for SBP and 10mmHg for DBP between both arms are present on 3 consecutive readings
  • If differences greater than 20mmHg for SBP and 10mmHg for DBP are present on 3 consecutive readings
  • impaired hepatic function
  • imapaired renal function
  • angioedema
  • aortic valvular stenosis or obstrcutive ejection disorder
  • primary hyperaldosteronism
  • renal transplantation, bilateral renal artery stenosis or unilateral stenosis in a single kidney, hemodialysis
  • severe respiratory disease
  • congestive heart failure( New York Association functional class Ⅲ or Ⅳ)
  • malignant hypertension
  • labile angina pectoris or myocardial infarction in the last 3 months before study entry

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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