Nifedipine GITS and Amlodipine Besylate on Recovery of Blood Pressure Rhythm and Arterial Stiffness

Phase 4TerminatedNCT02940548

Jing Liu99 enrolled

Overview

This trial evaluates the effects of Nifedipine GITS and Amlodipine besylate on blood pressure rhythm restoration and arterial stiffness in young and middle-aged non-dipper hypertensives. Half of participants will receive Nifedipine GITS, half of half will take medicine in the morning or at night. While the other half participants will take amlodipine besylate, whom will also be assigned taking medicine in the morning or at night. Ambulatory blood pressure monitoring and arterial stiffness examination will be performed before and after pharmaceutical intervention.

Written informed consent will obtained from all the participants. All the adverse reaction or adverse event, related or unrelated to the study drug, will be recorded in detail, including the occurrence time, symptoms and vital signs, degree, duration, laboratory test indexes, treatment methods and results, process, follow-up time, etc. If serious adverse event occurs, study drugs should be stopped and necessary remedy should be delivered immediately. At the same time, the investigator must report it to the local drug supervision, medical ethics committee and China Food and Drug Administration. \-

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

TREATMENT

Masking

NONE

Enrollment

Conditions

Hypertension

Interventions

Nifedipine GITSDRUG

Nifedipine GITS 30\~60mg/day for 8 weeks

Amlodipine besylateDRUG

Amlodipine besylate 5\~10mg/day for 8 weeks

Eligibility

Sex: ALLMin age: 18 YearsMax age: 65 Years

Medical Language ↔ Plain English

Inclusion Criteria: * Mild to moderate (Office blood pressure : 140 mmHg =\< systolic blood pressure (SBP) \<180 mmHg and / or 90 mmHg =\< diastolic blood pressure (DBP) \<110 mmHg) , non-dipper (ambulatory blood pressure monitoring (ABPM): night-time mean SBP / day-time mean SBP \>=0.9 and night-time mean SBP \>=120 mmHg) hypertensive subjects, who is drug treatment-naive or previously treated but discontinued for 2 weeks or more * The subject is voluntary to participate in the study and has signed the informed consent form Exclusion Criteria: * Known allergy to any component of Nifedipine and Amlodipine * Office SBP \>=180 mmHg and / or DBP \>=110 mmHg in the screening period * The patient who is taking calcium antagonists (monotherapy or combination with other drugs) * Evidences of secondary hypertension * History of cerebrovascular events, cardiac failure, serious coronary artery disease within 12 months * Type 1 diabetes mellitus (DM) * Severe liver diseases or renal insufficiency * The pregnant woman, the woman who may be pregnant or plan to be pregnant, or the lactating woman * The subject who needs to work at night (on night shift) * Other reasons that the subject can not participate in the study

Locations (1)

Peking University People's Hospital

Beijing, China

Outcomes

Primary Outcomes

Nighttime systolic blood pressure reduction

Compare the effects of two active drugs on nighttime systolic blood pressure reduction

Time frame: 8 weeks

Secondary Outcomes

The proportion of recovery of dipper rhythm of blood pressure

Compare the effects of two active drugs and different time administration on recovery of dipper rhythm. The proportion of blood pressure dipper rhythm at 8 weeks after two drugs administration will be calculated. The proportion of dipper rhythm at 8 weeks after two drugs administration in the morning or at night will also be calculated.

Time frame: 8 weeks

Change of pulse wave velocity

Compare the effects of two active drugs on pulse wave velocity(PWV). PWV will be measured before and after 8 weeks two active drugs administration.

Time frame: 8 weeks

Data from ClinicalTrials.gov

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