Antihypertensive Efficacy of Fixed Combination Drug
Primary Purpose
Hypertension
Status
Terminated
Phase
Phase 4
Locations
Israel
Study Type
Interventional
Intervention
Lercanidipine/enalapril fixed combination
Sponsored by

About this trial
This is an interventional treatment trial for Hypertension focused on measuring hypertension, Fixed combination, lercanidipine, enalapril, Blood Pressure Monitoring, Ambulatory
Eligibility Criteria
Inclusion Criteria:
- Essential hypertension at visit 1 defined as office blood pressure <140/90 mmHg and a 24 h ABPM >130/80 mmHg with a day time blood pressure (extracted from the 24h ABPM) >135/85 mmHg
- Male and female
- Age 18-80
- Every patient that in the medical opinion of the treating physician is eligible for Vasodip Combo 20 treatment.
- Willing to sign an informed consent
Exclusion Criteria:
- Use of more than 2 anti hypertensive medication at visit 1 (fixed combination is considered as two drugs)
- Mean 24 h ABPM values of more than 180/100 mmHg
- Pregnant women
- Women with potential age of pregnancy.
- Suspected secondary hypertension (investigator decision)
- Uncontrolled Diabetes Mellitus(investigator decision)
- Any of the following in the last six months: Myocardial Infarction, Stroke, Coronary by-pass surgery, Percutaneous coronariography with balloon dilation and/or stent insertion
- Congestive Heart Failure requiring pharmacological treatment
- Renal Failure, defined as serum creatinine equal or great than 1.5 mg% [confirmed twice] or hyperkalemia defined as serum potassium equal or great that 5 meq/l [confirmed twice]
- Malignancy that required Chemotherapy in the last 3 years.
- Any medical or none medical condition that in the eyes of the investigator will not allow the patient to complete the study.
Sites / Locations
- Clalit Health Services
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
lercanidipine-enalapril fixed combination
Arm Description
uncontrolled hypertensive patients will receive fixed combination therapy
Outcomes
Primary Outcome Measures
Blood Pressure control
Percentage of patients with controlled blood pressure with office BP and 24 h ABPM measurements, from baseline to week 4.
Secondary Outcome Measures
Full Information
NCT ID
NCT01211314
First Posted
September 28, 2010
Last Updated
June 26, 2016
Sponsor
Meir Medical Center
Collaborators
Dexcel Pharma Technologies Ltd.
1. Study Identification
Unique Protocol Identification Number
NCT01211314
Brief Title
Antihypertensive Efficacy of Fixed Combination Drug
Official Title
Treatment of Essential Hypertension With Vasodip-Combo 20. Efficacy and Safety Evaluation With 24 h Ambulatory Blood Pressure Measurements
Study Type
Interventional
2. Study Status
Record Verification Date
August 2011
Overall Recruitment Status
Terminated
Why Stopped
sponsor decision
Study Start Date
January 2011 (undefined)
Primary Completion Date
December 2011 (Actual)
Study Completion Date
April 2012 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Meir Medical Center
Collaborators
Dexcel Pharma Technologies Ltd.
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Treatment and control of hypertension is still insufficient. About 50% of the patients remain uncontrolled. Lack of compliance with discontinuation of drug treatment is an important reason for not achieving blood pressure. Several studies have shown that use of fixed combinations improve compliance significantly, by reducing the number of pill's intake.
This study will assess the antihypertensive efficacy of Vasodip-Combo 20® [enalapril 20 mg + lercanidipine 10 mg] as a fixed combination drug in uncontrolled antihypertensive patients.
Detailed Description
This is a single centre observational uncontrolled prospective study, Hypertensive patients that are either treatment naïve or uncontrolled on current therapy [one or two drugs] and meet all inclusion and exclusion criteria, will be assigned to Vasodip-Combo 20 as unique drug treatment. The treatment will then be continued for additional 4 weeks. Office blood pressure will be performed by the physician at each visit. 24 h. ambulatory blood pressure measurements [ABPM] and blood samples for electrolytes, creatinine and urea will be taken at base line visit and at at week 4.
Efficacy will be defined in terms of therapeutic goals expressed as target blood pressures according to World Health Organization and European society of Hypertension [ for office blood pressure and ambulatory blood pressure measurements] criteria:
Office Blood Pressure: Diastolic blood pressure ≤ 90 mmHg and Systolic blood pressure ≤ 140 mmHg for non-diabetics or Diastolic Blood Pressure ≤ 80 mmHg and Systolic Blood Pressure ≤ 130 mmHg for diabetics, respectively.
24 h Ambulatory Blood Pressure Measurements: 224 Hour: Diastolic Blood Pressure≤ 80 mmHg and Systolic Blood Pressure ≤ 130 mmHg, Awake time: Diastolic Blood Pressure ≤ 85 mmHg,Systolic Blood Pressure ≤ 135 mmHg Asleep Time: Diastolic Blood Pressure ≤70 mmHg, Systolic Blood Pressure ≤ 70 mmHg.
Effectiveness and Safety will also be evaluated taking into consideration patient compliance
Safety assessments:
Safety will be assessed by means of (S)Adverse effects reporting.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hypertension
Keywords
hypertension, Fixed combination, lercanidipine, enalapril, Blood Pressure Monitoring, Ambulatory
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
10 (Actual)
8. Arms, Groups, and Interventions
Arm Title
lercanidipine-enalapril fixed combination
Arm Type
Experimental
Arm Description
uncontrolled hypertensive patients will receive fixed combination therapy
Intervention Type
Drug
Intervention Name(s)
Lercanidipine/enalapril fixed combination
Other Intervention Name(s)
Vasodip Combo 20, hypertension, ambulatory blood pressure monitoring
Intervention Description
Lercanidipine 10 mg + enalapril 20 mg, once a day, used as a fixed combination drug. Unique dose during the study
Primary Outcome Measure Information:
Title
Blood Pressure control
Description
Percentage of patients with controlled blood pressure with office BP and 24 h ABPM measurements, from baseline to week 4.
Time Frame
Four weeks
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:
Essential hypertension at visit 1 defined as office blood pressure <140/90 mmHg and a 24 h ABPM >130/80 mmHg with a day time blood pressure (extracted from the 24h ABPM) >135/85 mmHg
Male and female
Age 18-80
Every patient that in the medical opinion of the treating physician is eligible for Vasodip Combo 20 treatment.
Willing to sign an informed consent
Exclusion Criteria:
Use of more than 2 anti hypertensive medication at visit 1 (fixed combination is considered as two drugs)
Mean 24 h ABPM values of more than 180/100 mmHg
Pregnant women
Women with potential age of pregnancy.
Suspected secondary hypertension (investigator decision)
Uncontrolled Diabetes Mellitus(investigator decision)
Any of the following in the last six months: Myocardial Infarction, Stroke, Coronary by-pass surgery, Percutaneous coronariography with balloon dilation and/or stent insertion
Congestive Heart Failure requiring pharmacological treatment
Renal Failure, defined as serum creatinine equal or great than 1.5 mg% [confirmed twice] or hyperkalemia defined as serum potassium equal or great that 5 meq/l [confirmed twice]
Malignancy that required Chemotherapy in the last 3 years.
Any medical or none medical condition that in the eyes of the investigator will not allow the patient to complete the study.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Eduardo Podjarny, MD
Organizational Affiliation
Clalit Health Services
Official's Role
Principal Investigator
Facility Information:
Facility Name
Clalit Health Services
City
Hertsliyah
State/Province
Hasharon
Country
Israel
12. IPD Sharing Statement
Plan to Share IPD
Yes
Citations:
PubMed Identifier
17209666
Citation
Hair PI, Scott LJ, Perry CM. Fixed-dose combination lercanidipine/enalapril. Drugs. 2007;67(1):95-106; discussion 107-8. doi: 10.2165/00003495-200767010-00007.
Results Reference
background
PubMed Identifier
18536784
Citation
Menne J, Haller H. Fixed-dose lercanidipine/enalapril for hypertension. Drugs Today (Barc). 2008 Apr;44(4):261-70. doi: 10.1358/dot.2008.44.4.1164756.
Results Reference
background
PubMed Identifier
20001654
Citation
Mancia G, Laurent S, Agabiti-Rosei E, Ambrosioni E, Burnier M, Caulfield MJ, Cifkova R, Clement D, Coca A, Dominiczak A, Erdine S, Fagard R, Farsang C, Grassi G, Haller H, Heagerty A, Kjeldsen SE, Kiowski W, Mallion JM, Manolis A, Narkiewicz K, Nilsson P, Olsen MH, Rahn KH, Redon J, Rodicio J, Ruilope L, Schmieder RE, Struijker-Boudier HA, Van Zwieten PA, Viigimaa M, Zanchetti A. Reappraisal of European guidelines on hypertension management: a European Society of Hypertension Task Force document. Blood Press. 2009;18(6):308-47. doi: 10.3109/08037050903450468. No abstract available.
Results Reference
background
Learn more about this trial
Antihypertensive Efficacy of Fixed Combination Drug
We'll reach out to this number within 24 hrs