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Treatment of Hypertension in Tibetan Adult Population

Primary Purpose

Hypertension

Status
Unknown status
Phase
Phase 4
Locations
China
Study Type
Interventional
Intervention
Nitrendipine
Hydrochlorothiazide
Captopril,Hydrochlorothiazide
Beijing hypotensive No.0
Sponsored by
West China Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Hypertension focused on measuring hypertension, Tibetan, Nitrendipine, hydrochlorothiazide, captopril, Beijing hypotensive No.0

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Adult Tibetan, who have been living in the Tibetan Plateau since he/she was born.
  2. Consistent with diagnosed hypertension, blood pressure, for 1-3 grade.
  3. Aged 18-80 years old.
  4. To sign informed consent.

Exclusion Criteria:

  1. diagnosis of secondary hypertension
  2. Hypertensive emergencies and urgencies
  3. Malignant hypertension
  4. Bilateral renal artery stenosis, Chronic Kidney Disease(CKD), serum creatinine> 133μmol / L.
  5. Suffering from congenital heart disease, rheumatic heart disease, hypertrophic cardiomyopathy, aortic stenosis.
  6. Occurred within the past 6 months who had a stroke or transient ischemic attack (TIA), unstable angina, myocardial infarction, percutaneous transluminal coronary angioplasty (PTCA).
  7. clinical significance of arrhythmia
  8. Active liver disease, history of chronic persistent hepatitis, alanine aminotransferase(ALT)> upper limit of normal.
  9. Pregnancy, pregnancy or breast-feeding women to prepare.

Sites / Locations

  • West China Hospital

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Experimental

Experimental

Experimental

Experimental

Arm Label

A1 nitrendipine

A2 hydrochlorothiazide

B1 captopril plus Hydrochlorothiazide

B2 Beijing hypotensive No.0

Arm Description

this arm will include Tibetan patients with hypertension whose BP is higher than 140/90mmHg but lower than 160/100mmHg and nitrendipine will be added (dose range 10mg-20mg bid).

this arm will include Tibetan patients with hypertension whose BP is higher than 140/90mmHg but lower than 160/100mmHg and hydrochlorothiazide will be added (dose range 12.5mg-25mg)

this arm will include Tibetan patients with hypertension whose BP is higher than 160/100mmHg and captopril plus Hydrochlorothiazide will be added (dose range:captopril 25mg-50mg tid, Hydrochlorothiazide 12.5mg-25mg qd).

this arm will include Tibetan patients with hypertension whose BP is higher than 160/100mmHg and Beijing hypotensive will be added (dose range:Beijing hypotensive No.0 one pile qd or less ).

Outcomes

Primary Outcome Measures

Change of Blood Pressure
Change of systolic blood pressure,diastolic blood pressure and mean arterial pressure from baseline to study end at 12 months.

Secondary Outcome Measures

Change of target organ damage
Change of target organ damage(including estimated glomerular filtration rate, microalbuminuria, carotid intima-media thickness, arterial stiffness, left ventricular mass index) from baseline to study end at 12 months.

Full Information

First Posted
August 13, 2014
Last Updated
August 28, 2014
Sponsor
West China Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT02217852
Brief Title
Treatment of Hypertension in Tibetan Adult Population
Official Title
A Randomized, Open-label, Positive Drug Controlled Clinical Trials to Compare the Efficacy of Nitrendipine and Hydrochlorothiazide , Captopril Plus Hydrochlorothiazide and Beijing Hypotensive No.0 in Tibetan Hypertension
Study Type
Interventional

2. Study Status

Record Verification Date
August 2014
Overall Recruitment Status
Unknown status
Study Start Date
August 2014 (undefined)
Primary Completion Date
January 2016 (Anticipated)
Study Completion Date
July 2016 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
West China Hospital

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Several surveys had revealed that Tibetan adults had high prevalence of hypertension. However, there was no research studying the antihypertensive effect of the known drugs in Tibetan. The main arms of our study were to determine if the efficacy of lowing blood pressure and protecting target organ damage differs between nitrendipine and Hydrochlorothiazide in mild hypertension in Tibetan, and to determine if the efficacy of lowing blood pressure and protecting target organ damage differs between captopril plus Hydrochlorothiazide and Beijing hypotensive No.0 in moderate and severe Tibetan hypertension.
Detailed Description
Several surveys had revealed that Tibetan adults had high blood pressure(BP)and prevalence of hypertension than other parts of China and were also higher than those in developed nations as well. For example, one study found that among Tibetan herdsmen 40 years and older, the prevalence of hypertension was 56% and the mean systolic blood pressure/diastolic blood pressure was 146.6/92.0mmHg. However, the rates of awareness, treatment, and control were dismally low. The Tibetan have been living in the Tibetan Plateau. The special natural and social environment there,as well as ethnic ,may all be involved in the etiology of the high prevalence and effect the response to antihypertensive treatment. Nevertheless, few interventional studies have been done in Tibetan hypertensive patients. Therefore, the purpose of our study was to compare the blood pressure reduction between different antihypertensive drugs. Nitrendipine, hydrochlorothiazide, captopril and Beijing hypotensive No.0 (also named" compound hypotensive tablet") are selected, which are cheap and available in the Tibetan Plateau. Nitrendipine, hydrochlorothiazide and captopril are the representatives of Dihydropyridines Calcium antagonists, diuretics, and angiotensin-converting enzyme inhibitors, respectively. They are all recommended as the first-line antihypertensive drug. Beijing hypotensive No.0 is produce by China Resources Double-crane Pharmaceutical company in China, and it is a fixed-dose combination containing reserpine 0.1mg, hydrochlorothiazide 12.5mg, dihydralazine sulfate 12.5mg, triamterene 12.5mg. Many studies conducted in China have demonstrated its efficacy and safety in lowing blood pressure. After recruitment, participant will be grouped according to their BP. If BP<160/100mmHg, monotherapy is started. Patient is randomly assigned to receive nitrendipine 10mg bid or Hydrochlorothiazide 12.5mg qd. If BP≥160/100mmHg, Patient is randomly assigned to receive two drug combination therapy(captopril 25mg three times daily (tid) and Hydrochlorothiazide 12.5mg qd) or Beijing hypotensive No.0 one pile qd. During the following 12 months,each participant will take at least four visits at 1、3、6 and 12 months respectively. Goal BP for all participants was less than 140/90mmHg, achieved by titrating the assigned study drug and adding open-label agents when necessary. The maximum dosage is 20mg BID for nitrendipine, 25mg qd for Hydrochlorothiazide and 50mg tid for captopril. The dosage of Beijing hypotensive No.0 should not be added.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hypertension
Keywords
hypertension, Tibetan, Nitrendipine, hydrochlorothiazide, captopril, Beijing hypotensive No.0

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
800 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
A1 nitrendipine
Arm Type
Experimental
Arm Description
this arm will include Tibetan patients with hypertension whose BP is higher than 140/90mmHg but lower than 160/100mmHg and nitrendipine will be added (dose range 10mg-20mg bid).
Arm Title
A2 hydrochlorothiazide
Arm Type
Experimental
Arm Description
this arm will include Tibetan patients with hypertension whose BP is higher than 140/90mmHg but lower than 160/100mmHg and hydrochlorothiazide will be added (dose range 12.5mg-25mg)
Arm Title
B1 captopril plus Hydrochlorothiazide
Arm Type
Experimental
Arm Description
this arm will include Tibetan patients with hypertension whose BP is higher than 160/100mmHg and captopril plus Hydrochlorothiazide will be added (dose range:captopril 25mg-50mg tid, Hydrochlorothiazide 12.5mg-25mg qd).
Arm Title
B2 Beijing hypotensive No.0
Arm Type
Experimental
Arm Description
this arm will include Tibetan patients with hypertension whose BP is higher than 160/100mmHg and Beijing hypotensive will be added (dose range:Beijing hypotensive No.0 one pile qd or less ).
Intervention Type
Drug
Intervention Name(s)
Nitrendipine
Intervention Description
doses used range from 10-20mg po bid. Total duration would be until completion or study or medication intolerance.
Intervention Type
Drug
Intervention Name(s)
Hydrochlorothiazide
Intervention Description
doses used range from 12.5-25mg po qd. Total duration would be until completion or study or medication intolerance.
Intervention Type
Drug
Intervention Name(s)
Captopril,Hydrochlorothiazide
Intervention Description
doses used range from 25-50mg po tid for captopril and 12.5-25mg po qd for hydrochlorothiazide. Total duration would be until completion or study or medication intolerance.
Intervention Type
Drug
Intervention Name(s)
Beijing hypotensive No.0
Other Intervention Name(s)
compound hypotensive tablet
Intervention Description
1 pile po qd or less. Total duration would be until completion or study or medication intolerance.
Primary Outcome Measure Information:
Title
Change of Blood Pressure
Description
Change of systolic blood pressure,diastolic blood pressure and mean arterial pressure from baseline to study end at 12 months.
Time Frame
12 months
Secondary Outcome Measure Information:
Title
Change of target organ damage
Description
Change of target organ damage(including estimated glomerular filtration rate, microalbuminuria, carotid intima-media thickness, arterial stiffness, left ventricular mass index) from baseline to study end at 12 months.
Time Frame
12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Adult Tibetan, who have been living in the Tibetan Plateau since he/she was born. Consistent with diagnosed hypertension, blood pressure, for 1-3 grade. Aged 18-80 years old. To sign informed consent. Exclusion Criteria: diagnosis of secondary hypertension Hypertensive emergencies and urgencies Malignant hypertension Bilateral renal artery stenosis, Chronic Kidney Disease(CKD), serum creatinine> 133μmol / L. Suffering from congenital heart disease, rheumatic heart disease, hypertrophic cardiomyopathy, aortic stenosis. Occurred within the past 6 months who had a stroke or transient ischemic attack (TIA), unstable angina, myocardial infarction, percutaneous transluminal coronary angioplasty (PTCA). clinical significance of arrhythmia Active liver disease, history of chronic persistent hepatitis, alanine aminotransferase(ALT)> upper limit of normal. Pregnancy, pregnancy or breast-feeding women to prepare.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Xiaoping Chen, MD
Phone
86-028-85422175
Email
xiaopingchen11@126.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Xiaoping Chen, MD
Organizational Affiliation
West China Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
West China Hospital
City
Chengdu
State/Province
Sichuan
ZIP/Postal Code
610041
Country
China

12. IPD Sharing Statement

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Treatment of Hypertension in Tibetan Adult Population

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