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Sponsors and Collaborators: |
University of Split Dr Ivancica Pavlicevic Family Practice Office |
Information provided by: | University of Split |
ClinicalTrials.gov Identifier: | NCT00631514 |
NSAIDs may increase blood pressure and blunt the effects of many antihypertensives. Members of these drug classes differ in their propensity to such an interaction.
Condition | Intervention | Phase |
Hypertension |
Drug: acetaminophen Drug: ibuprofen Drug: piroxicam |
Phase IV |
MedlinePlus related topics: | High Blood Pressure |
Drug Information available for: | Ibuprofen Dexibuprofen Acetaminophen Piroxicam |
Study Type: | Interventional |
Study Design: | Treatment, Randomized, Single Blind (Outcomes Assessor), Active Control, Factorial Assignment, Efficacy Study |
Official Title: | Relevance of the Interaction Between Antihypertensive and Antirheumatic Drugs in a Family Practice |
Enrollment: | 88 |
Study Start Date: | January 2005 |
Study Completion Date: | September 2006 |
Primary Completion Date: | September 2006 (Final data collection date for primary outcome measure) |
Arms | Assigned Interventions |
1: No Intervention
Hypertensive persons taking either lisinopril/hydrochlorothiazide fixed combination or amlodipine all the time.
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2: Experimental
Intervention: NSAID. Hypertensives with osteoarthritis taking already amlodipine (5-10 mg o.d. per os) were randomized to the following drug interventions: to take either acetaminophen (1000 mg t.i.d. per os), piroxicam (10-20 mg o.d. per os) or ibuprofen (400-600 mg t.i.d. per os) for 1 month
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Drug: acetaminophen
acetaminophen 1000 mg t.i.d. per os ibuprofen 400-600 mg t.i.d. per os piroxicam 10-20 mg o.d. per os
Drug: ibuprofen
acetaminophen 1000 mg t.i.d. per os ibuprofen 400-600 mg t.i.d. per os piroxicam 10-20 mg o.d. per os
Drug: piroxicam
acetaminophen 1000 mg t.i.d. per os ibuprofen 400-600 mg t.i.d. per os piroxicam 10-20 mg o.d. per os
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3: Experimental
Hypertensives with osteoarthritis taking already lisinopril/hydrochlorothiazide (20/12.5 mg o.d. per os), were sequentially randomized to the following drug interventions: acetaminophen (1000 mg t.i.d.), ibuprofen (400-600 mg t.i.d.) or piroxicam (10-20 mg o.d.), for 1 month each
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Drug: acetaminophen
acetaminophen 1000 mg t.i.d. per os ibuprofen 400-600 mg t.i.d. per os piroxicam 10-20 mg o.d. per os
Drug: ibuprofen
acetaminophen 1000 mg t.i.d. per os ibuprofen 400-600 mg t.i.d. per os piroxicam 10-20 mg o.d. per os
Drug: piroxicam
acetaminophen 1000 mg t.i.d. per os ibuprofen 400-600 mg t.i.d. per os piroxicam 10-20 mg o.d. per os
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To compare prospectively the effects of piroxicam, ibuprofen and acetaminophen on blood pressure control in hypertensive patients with osteoarthritis.
Ages Eligible for Study: | 55 Years to 78 Years |
Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Exclusion Criteria:
Croatia | |||||
Split University School of Medicine. Family Practice Department | |||||
Split, Croatia, 21000 |
University of Split |
Dr Ivancica Pavlicevic Family Practice Office |
Study Director: | Zvonko - Rumboldt, MD, PhD | Split University School of Medicine |
Split University School of Medicine 
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Responsible Party: | Split University School of Medicine ( Ivancica Pavlicevic ) |
Study ID Numbers: | 1-Pavlicevic |
First Received: | February 27, 2008 |
Last Updated: | March 7, 2008 |
ClinicalTrials.gov Identifier: | NCT00631514 |
Health Authority: | Croatia: National Ethics Committee; Zagreb, Croatia |
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