Effect of Nifedipine GITS in Patients With Mild-to-moderate Primary Hypertension

Peking University First Hospital700 enrolled

Overview

This is a multi-center, open-label, observational study. The aim of this study is to evaluate the efficacy of Nifedipine GITS on lowering blood pressure in Chinese adults with mild-to-moderate hypertension.

The primary aim of the study is to evaluate the efficacy of nifedipine gastrointestinal therapeutic system (GITS) on lowering blood pressure in Chinese adults with mild-to-moderate hypertension. The secondary aim of the study is to evaluate the efficacy of Nifedipine GITS on lowering blood pressure in hypertensive patients with different urinary sodium levels. Based on sample size estimation, the plan is to recruit 700 patients from 16 centers. At baseline, patients'demographic characters, disease history and anthropometric indices will be collected, laboratory tests will be performed for blood routine examination, urinalysis, renal function, hepatic function, urinary sodium and 24-hour urinary sodium. All eligible patients will be assigned to a treatment of Nifedipine GITS and followed up for 8 weeks. At 0 day, 2,weeks, 4 weeks and 8 weeks of the study, seated blood pressure, vital signs, medication and adverse events were collected. At the end of the study, 24-hour ambulatory blood pressure monitoring (ABPM) will be performed for all participants.

Study Type

INTERVENTIONAL

Allocation

Purpose

TREATMENT

Masking

NONE

Enrollment

700

Conditions

Hypertension

Interventions

Nifedipine GITSDRUG

Eligibility

Sex: ALLMin age: 18 YearsMax age: 75 Years

Medical Language ↔ Plain English

Inclusion Criteria: * a seated systolic BP (SBP) ≥140 mmHg and \<180 mmHg and/or a seated diastolic BP (DBP) ≥90 mmHg and \<110 mmHg; * an age ≥18 and ≤75 years; * those who had not taken any BP-lowering medications in 1 month before the study. Exclusion Criteria: * a seated systolic BP (SBP) ≥180 mmHg and/or a seated diastolic BP ≥110 mmHg; * secondary hypertension; * diagnosed heart failure or stroke; * Any of alanine aminotransferase (ALT) or aspartate aminotransferase (AST) was above 1.5 times of it's normal value upper limit, Serum creatinine \>177 µmmol/L (2mg/dL), or liver cirrhosis; * subjects with carotid stenosis or systolic murmur * subjects with a history of unstable angina pectoris, acute mycardial infarction, percutaneous transluminal coronary angiography or coronary artery bypass grafting in the past 6 months; * subjects who were within lactation period, pregnant, or planning to become pregnant during the study; * hypersensitive to Nifedipine GITS or with SAE; * subjects who are participating in other clinical trials; * considered not fit for the study due to other reasons according to the researchers (such as Malignant tumor, psyche or nervous system dysfunction, or special diseases).

Locations (1)

Division of Cardiology, Peking University First Hospital

Beijing, China

RECRUITING

Outcomes

Primary Outcomes

Control rate of hypertension evaluated by office blood pressure at 8 weeks

Time frame: 8 weeks

Control rate of hypertension evaluated by office blood pressure at 4 weeks

Time frame: 4 weeks

Control rate of hypertension evaluated by office blood pressure at 2 weeks

Time frame: 2 weeks

Secondary Outcomes

Control rate of hypertension evaluated by 24-hour ABPM at 8 weeks

Time frame: 8 weeks

Change of office blood pressure from baseline to 8 weeks

Time frame: 8 weeks

Change of 24-hour ABPM from baseline to 8 weeks

Time frame: 8 weeks

Central Contacts

Yang Yu, MD

CONTACT

8610-83575262 jiyou_2000@163.com

Data from ClinicalTrials.gov

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