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Effect of Fully Blocking Type 1 Angiotensin Receptor on Target Organ Damage of Postmenopausal Hypertensive Women

L

Lanzhou University

Status

Unknown

Conditions

Hypertension

Treatments

Drug: Valsartan 1
Drug: Valsartan 80 mg

Study type

Interventional

Funder types

Other

Identifiers

NCT03432468
LanZhouU

Details and patient eligibility

About

This study compared the improvements of blood pressure levels, left ventricular hypertrophy, left ventricular diastolic function, vascular function and cognitive function between postmenopausal hypertensive women and age-matched hypertensive male patients through the evaluation of the effects of fully blocked AT1 receptor by valsartan. Additionally, the differences of the above indexes between the patients who were fully blocked AT1 receptor by valsartan and the patients who were treated with a single dose of valsartan treatment were assessed, so as to provide theory basis for clinical treatment of postmenopausal hypertensive women.

Enrollment

102 estimated patients

Sex

All

Ages

40 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Clinical diagnosis of hypertension
  • Women are all postmenopausal
  • Must provide written informed consent

Exclusion criteria

  • Secondary hypertension
  • Coronary disease
  • Heart failure
  • Arterial fibrillation
  • Previous myocardial infarction
  • Previous stroke
  • Malignant disease
  • Kidney failure
  • Liver failure
  • Neoplastic disease
  • Severe neurological diseases
  • Severe metabolic or organic decompensation
  • Refuse to sign the informed consent form

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

102 participants in 2 patient groups, including a placebo group

postmenopausal hypertensive women
Active Comparator group
Treatment:
Drug: Valsartan 1
Drug: Valsartan 80 mg
age-matched hypertensive male patients
Placebo Comparator group
Treatment:
Drug: Valsartan 1

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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