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Treatment of Hypertension in Tibetan Adult Population

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

Status
UNKNOWN
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02217852
Enrollment
800
Registered
2014-08-15
Start date
2014-08-31
Completion date
2016-07-31
Last updated
2014-08-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hypertension

Keywords

hypertension, Tibetan, Nitrendipine, hydrochlorothiazide, captopril, Beijing hypotensive No.0

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.

Interventions

doses used range from 10-20mg po bid. Total duration would be until completion or study or medication intolerance.

DRUGHydrochlorothiazide

doses used range from 12.5-25mg po qd. Total duration would be until completion or study or medication intolerance.

DRUGCaptopril,Hydrochlorothiazide

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.

DRUGBeijing hypotensive No.0

1 pile po qd or less. Total duration would be until completion or study or medication intolerance.

Sponsors

West China Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

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.

Design outcomes

Primary

MeasureTime frameDescription
Change of Blood Pressure12 monthsChange of systolic blood pressure,diastolic blood pressure and mean arterial pressure from baseline to study end at 12 months.

Secondary

MeasureTime frameDescription
Change of target organ damage12 monthsChange 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.

Countries

China

Contacts

Primary ContactXiaoping Chen, MD
xiaopingchen11@126.com86-028-85422175

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026