Comparative Study of the Effects of Telmisartan and Nebivolol

NCT ID: NCT02057328

Last Updated: 2014-02-07

Basic Information

• Recruitment Status: UNKNOWN
• Clinical Phase: PHASE4
• Total Enrollment: 80 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2010-12-31
• Study Completion Date: 2017-01-31

Brief Summary

Τhe effectiveness of newer angiotensin-II receptor blockers and cardioselective beta-adrenergic blockers in treatment of arterial hypertension and in improvement of arterial stiffness has been established in previous studies among the hypertensive population. The present study is a comparison of the performance of two drugs, telmisartan and nebivolol, in 24h ambulatory blood pressure values and in the degree of arterial stiffness of patients with stage I arterial hypertension.

Measurements will be carried out with the use of 24-h ambulatory blood pressure measurement devices and the method of pulse-wave velocity analysis. The effects of telmisartan and nebivolol are going to be compared for a total time period of 12 months.

The aim of this project is to determine whether the expected decrease in arterial stiffness of subjects with stage I arterial hypertension can be attributed to the blood pressure fall solely, or to other factors as well. These factors are possibly dependent on the action of these drugs on the renin-angiotensin II-aldosterone system (RAAS) or on peripheral vasodilatory actions.

The present study is going to be the first comparative test of the anti-hypertensive effects of the two pharmaceutical substances in 12 months' time, and of the elimination of total cardiovascular risk in terms of primary prevention of cardiovascular attacks.

Detailed Description

INTRODUCTION

We intend to study the effects of telmisartan, a newer angiotensin-II receptor blocker and nebivolol, a cardioselective beta-adrenergic blocker on the 24-h ambulatory blood pressure values of subjects with stage I arterial hypertension in a total time period of 12 months. At the same time, a study of the effects of treatment with the above mentioned antihypertensive drugs on the grade of arterial stiffness of hypertensive subjects will be carried out. The purpose of this project is to determine whether the expected decrease in arterial stiffness of subjects with stage I arterial hypertension can be attributed to the blood pressure fall solely, or to other factors, as well. These factors are possibly dependent on the action of these drugs on the renin-angiotensin II-aldosterone system (RAAS) or on peripheral vasodilatory actions.

The objective of the study is to observe and compare, in a time period of 12 months, the performance of two antihypertensives of different drug categories, telmisartan and nebivolol, in treatment of patients with stage I arterial hypertension and in improvement of arterial stiffness. It is an observational study according to the ESH (European Society of Hypertension) guidelines for treatment of patients with arterial hypertension.

METHODS

Study population

The study is going to be applied to subjects that attend the Hypertension-ABPM Clinic of the 3rd department of Internal Medicine in Papageorgiou University Hospital. All individuals enrolled in the study will give a written consent for their participation. Healthy volunteers aged between 18 and 65 years diagnosed with stage I arterial hypertension (24h SBP/DBP ≥ 130/80 mm Hg) will be selected. All cases will regard to the initial diagnosis of arterial hypertension, for which participants in the study will not receive or have previously received any antihypertensive medication. At attendance, individual body weight in light clothing and without shoes is going to be recorded and BMI (body mass index) is going to be calculated as the ratio "body weight (kg) / [height (cm)]2 " . Waist and hip circumference will also be measured in cm. Participants in the study will be divided into three categories according to BMI: Normal weight (BMI 18,5 to 24,9), overweight (BMI 25 to 29,9) and obese (BMI over 30). Detailed case-history and family history, smoking habit and alcohol use will be recorded for each individual. A series of laboratory examinations will be executed: Hct, serum glucose, fasting serum total cholesterol, HDL, LDL and triglycerides, plasma urea, creatinine, uric acid, sodium, potassium.

All participants in the study are going to be patients initially instructed for a three-month lifestyle modification, according to the ESH guidelines. Recommended interventions include cessation of smoking, physical exercise 3-4 hours per week, exclusion of polyunsaturated fatty acids from the diet, high contamination of natural fibers, reduction of added salt to a minimum, all aiming to reduce blood pressure to normal. Patients who present with stage I arterial hypertension (24h SBP/DBP ≥ 130/80 mm Hg) at the end of the three-month period of lifestyle modification will enter the study and undergo PWV-measurement, according to the methods described below.

The final selection of the sample of 80 patients diagnosed with stage I arterial hypertension will be based on the ABPM results (24h SBP/DBP ≥ 130/80 mm Hg). Patients who present with normal ABPM values at the end of the 3-month period will be excluded from the study. Subjects diagnosed with white-coat hypertension [increased office BP values (SBP/DBP ≥ 140/90 mm Hg) combined with normal ABPM values (24h SBP/DBP < 130/80 mm Hg)] will also be excluded from the study.

Exclusion criteria: All subjects with contra-indications for submission of drugs used in the research protocol are going to be excluded from the study. The following categories of patients will not participate in the research: renal failure, hepatic failure, renal artery stenosis, bronchial asthma, vasoconstrictive (Prinzmetal's) angina, hypertrophic cardiomyopathy, aortic valve stenosis, mitral valve stenosis, sinus tachycardia, sinus bradycardia, sick sinus syndrome, Wolff-Parkinson-White syndrome, chronic atrial fibrillation, second and third degree atrioventricular block, right heart failure due to pulmonary hypertension, pheochromocytoma, peripheral artery disease. Pregnant and nursing women will be excluded from the study (history and pregnancy test).

At the beginning of Phase I (time 0), patients will be randomized into two groups, according to the antihypertensive medication they are going to receive. The first group will receive telmisartan, whereas the second group of patients will be instructed to receive nebivolol. In the telmisartan group, each patient will receive 40 mg of telmisartan daily in the morning. Patients of the group of nebivolol will take 5 mg of nebivolol daily in the morning. The aim of the study in each of the phases is the normalization of the BP of the participants (24h SBP/DBP < 130/80 mm Hg).

At the end of the first month of treatment, all participants will undergo 24h ABPM and arterial stiffness measurement. Patients classified in the normal BP range based on the results of ABPM (24h SBP/DBP < 130/80 mm Hg) will continue on the same medication scheme. For patients still classified in the stage I hypertensive range, the treatment will be modulated as follows: the telmisartan group is going to receive 80 mg of telmisartan daily in the morning, while the nebivolol group will receive 10 mg of nebivolol daily in the morning (beginning of Phase II - time 1 month).

The same procedure (24h ABPM and arterial stiffness measurement) will be repeated at the end of the 6th month from the beginning of the study. Patients classified in the normal BP range based on the results of ABPM (24h SBP/DBP < 130/80 mm Hg) will continue on the same medication scheme. For patients still classified in the stage I hypertensive range, the treatment will be modulated as follows: 12,5 mg of hydrochlorothiazide will be added in the medication scheme of both groups. The telmisartan group starts to receive the combination scheme telmisartan/HCTZ 80/12,5 mg morning dose, whereas the nebivolol group starts on the combination scheme nebivolol/HCTZ 10/12,5 mg morning dose. This point indicates the beginning of phase III of the study (time 6 months). When 12 months from the beginning of the study are completed, patients of both groups will undergo 24h ABPM and arterial stiffness measurement. The end of the 12-month period from the beginning of the study (end of Phase III) indicates the completion of the project.

Analysis of the measurement methods

24-h ABPM 24-h ABPM will be performed for all participants on a typical working day. All subjects will be instructed to follow their usual program of daily activities. The measurement device Spacelabs 90217 (Spacelabs Inc., Redmond, Wash.) will be used. A cuff of the appropriate diameter will be adapted around the non-dominant arm of each subject and three BP measurements will take place. A simultaneous measurement with the use of a sphygmomanometric device will be taken, in order to make sure that the mean of differences in BP values with the two methods is not ≥ 5 mm Hg. All participants should maintain their normal activity from 08:00 to 22:00, with the arm still and loose during the measurements. One measurement takes place every 15 minutes between 06:00 and 00:00, and every 30 minutes between 00:00 and 06:00. Participants should avoid intense physical exercise and sleep during daytime, while they will be instructed to rest between 00:00 and 06:00 and not to rise out of bed until 06:00, even if awakened before that time.

Arterial stiffness measurement

The measurement of the grade of arterial stiffness of the participants will take place in each phase of the study in a quiet examination room with stable temperature (21ºC) and low lighting. Subjects are instructed to lie down at the examination room for 15 minutes before the beginning of the procedure. Also, they should avoid food, caffeine and cigarette smoking for three hours, and alcohol use for ten hours before the measurement. The method of the measurement of the carotid-femoral pulse wave velocity (PWV), according to the European Expert Consensus on Arterial Stiffness, is used to define the grade of arterial stiffness. The velocity of the pulse wave (PWV) is calculated by the equation PWV= D (m) / t (s), (t) representing the time needed for transmission of the arterial pulse wave across the distance, and (D) representing the distance between the measurement points. (D) is directly measured with the use of a measurement tape, whereas (t) is given by the Complior System (Colson, Les Lilas, France). It is quantified as the time space between the transmission of the pulse from carotid to radial and to femoral artery and the formation of the two waveforms, respectively. The two waveforms are simultaneously recorded at the right common carotid artery and the right femoral artery ('foot to foot' method) via mechanic sensors put on the body surface in direct contact with the skin. Participants should stay in supine position and avoid talking or sleeping during the recordings. All the measurements will be executed by the same observer. A second measurement of the PWV will be carried out 15 minutes after the first one. The two recordings will be identically carried out.

Conditions

Hypertension

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

NEBIVOLOL

Patients of the group of nebivolol will take 5 mg of nebivolol daily in the morning. At the end of the first month of treatment, patients classified in the normal BP range based on the results of ABPM (24h SBP/DBP \< 130/80 mm Hg) will continue on the same medication scheme. Patients still classified in the stage I hypertensive range the nebivolol group will receive 10 mg of nebivolol daily in the morning. At the end of the 6th month patients classified in the normal BP range based on the results of ABPM will continue on the same medication scheme. Patients classified in the stage I hypertensive range 12,5 mg hydrochlorothiazide will be added. The end of the 12-month period from the beginning of the study indicates the completion of the project.

Group Type: ACTIVE_COMPARATOR

NEBIVOLOL

Intervention Type: DRUG

Patients will take 5 mg of nebivolol daily in the morning. At the end of the first month of treatment, patients classified in the normal BP range based on the results of ABPM will continue on the same medication scheme. Patients classified in the stage I hypertensive range the nebivolol group will receive 10 mg of nebivolol daily in the morning. At the end of the 6th month from the beginning of the study patients classified in the normal BP range based on the results of ABPM will continue on the same medication scheme. For patients classified in the stage I hypertensive range 12,5 mg of hydrochlorothiazide will be added. The end of the 12-month period from the beginning of the study indicates the completion of the project

TELMISARTAN

Patients of the group of telmisartan will take 40 mg of telmisarta daily in the morning. At the end of the first month of treatment, patients classified in the normal BP range based on the results of ABPM (24h SBP/DBP \< 130/80 mm Hg) will continue on the same medication scheme. Patients classified in the stage I hypertensive range will receive 80 mg of telmisartan daily in the morning. The same procedure will be repeated at the end of the 6th month from the beginning of the study. Patients classified in the normal BP range will continue on the same medication scheme. For patients still classified in the stage I hypertensive range12,5 mg of hydrochlorothiazide will be added. The end of the 12-month period from the beginning of the study indicates the completion of the project.

Group Type: ACTIVE_COMPARATOR

TELMISARTAN

Intervention Type: DRUG

Patients of the group of telmisartan will take 40 mg of telmisartan daily in the morning. At the end of the first month of treatment, patients classified in the normal BP range based on the results of ABPM will continue on the same medication scheme. Patients still classified in the stage I hypertensive range will receive 80 mg of telmisartan daily in the morning. At the end of the 6th month from the beginning of the study patients classified in the normal BP range will continue on the same medication scheme. For patients still classified in the stage I hypertensive range12,5 mg of hydrochlorothiazide will be added. The end of the 12-month period from the beginning of the study indicates the completion of the project.

Interventions

TELMISARTAN

Patients of the group of telmisartan will take 40 mg of telmisartan daily in the morning. At the end of the first month of treatment, patients classified in the normal BP range based on the results of ABPM will continue on the same medication scheme. Patients still classified in the stage I hypertensive range will receive 80 mg of telmisartan daily in the morning. At the end of the 6th month from the beginning of the study patients classified in the normal BP range will continue on the same medication scheme. For patients still classified in the stage I hypertensive range12,5 mg of hydrochlorothiazide will be added. The end of the 12-month period from the beginning of the study indicates the completion of the project.

Intervention Type: DRUG

NEBIVOLOL

Patients will take 5 mg of nebivolol daily in the morning. At the end of the first month of treatment, patients classified in the normal BP range based on the results of ABPM will continue on the same medication scheme. Patients classified in the stage I hypertensive range the nebivolol group will receive 10 mg of nebivolol daily in the morning. At the end of the 6th month from the beginning of the study patients classified in the normal BP range based on the results of ABPM will continue on the same medication scheme. For patients classified in the stage I hypertensive range 12,5 mg of hydrochlorothiazide will be added. The end of the 12-month period from the beginning of the study indicates the completion of the project

Intervention Type: DRUG

Other Intervention Names

MICARDIS; LOBIVON

Eligibility Criteria

Exclusion Criteria

Patients who present with normal ABPM values at the end of the 3-month period will be excluded from the study. Subjects diagnosed with white-coat hypertension [increased office BP values (SBP/DBP ≥ 140/90 mm Hg) combined with normal ABPM values (24h SBP/DBP < 130/80 mm Hg)] will also be excluded from the study.

All subjects with contra-indications for submission of drugs used in the research protocol are going to be excluded from the study. The following categories of patients will not participate in the research: renal failure, hepatic failure, renal artery stenosis, bronchial asthma, vasoconstrictive (Prinzmetal's) angina, hypertrophic cardiomyopathy, aortic valve stenosis, mitral valve stenosis, sinus tachycardia, sinus bradycardia, sick sinus syndrome, Wolff-Parkinson-White syndrome, chronic atrial fibrillation, second and third degree atrioventricular block, right heart failure due to pulmonary hypertension, pheochromocytoma, peripheral artery disease. Pregnant and nursing women will be excluded from the study (history and pregnancy test).

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 65 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Aristotle University Of Thessaloniki

OTHER

Sponsor Role: lead

Responsible Party

Vasilios Kotsis

PROF. MEDICINE

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Sofia Papakatsika, MD

Role: PRINCIPAL_INVESTIGATOR

AUTH

Vasilios Kotsis, MD,Ph.D

Role: STUDY_CHAIR

AUTH

Locations

Hypertension-ABPM Center 3rd department of Internal Medicine

Thessaloniki, , Greece

Site Status: RECRUITING

Countries

Greece

Central Contacts

Vasilios Kotsis, MD,Ph.D

Role: CONTACT

vkotsis@auth.gr

+306974748860

Facility Contacts

Vasilios Kotsis, MD, Ph.D

Role: primary

vkotsis@auth.gr

+306974748860

Other Identifiers

TELNEB

Identifier Type: -

Identifier Source: org_study_id