Ambulatory Blood Pressure Monitoring in the Prediction of Cardiovascular Events and Effects of Chronotherapy
NCT00295542 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 3344
Last updated 2009-04-28
Summary
The MAPEC study was designed to investigate whether normalizing the circadian blood pressure profile towards a more dipper pattern (increasing the diurnal/nocturnal ratio of blood pressure) by the use of Chronotherapy (that is, taking into account the time of day of administration of antihypertensive medications) reduces cardiovascular risk.
Conditions
Interventions
- DEVICE
-
Ambulatory blood pressure monitoring
Sampling at 20-min intervals from 07:00 to 23:00 hours and at 30-min intervals at night for 48 consecutive hours
- PROCEDURE
-
Chronotherapy, timing of antihypertensive medication
Comparison of effects of awakening versus bedtime dosing
- DRUG
-
ACEI (including spirapril, enalapril, quinapril, lisinopril)
Treatment at awakening versus bedtime
- DRUG
-
ARB (including valsartan, telmisartan, olmesartan)
Treatment at awakening versus bedtime
- DRUG
-
beta blockers (including nebivolol, atenolol, carvedilol)
Treatment at awakening versus bedtime
- DRUG
-
diuretics (torasemide, indapamide, HTCZ) and doxazosin
Treatment at awakening versus bedtime
- PROCEDURE
-
Combination therapy in essential hypertension
Treatment at awakening versus bedtime
Sponsors & Collaborators
-
Hospital Clinico Universitario de Santiago
collaborator OTHER -
Ministry of Work and Welfare - Xunta de Galicia
collaborator OTHER_GOV -
Ministerio de Educacion y Ciencia, Spain
collaborator UNKNOWN -
University of Vigo
lead OTHER
Principal Investigators
-
Ramon C Hermida, PhD · University of Vigo
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2000-03-31
- Primary Completion
- 2009-04-30
- Completion
- 2009-04-30
Countries
- Spain
Study Locations
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