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Trial details imported from ClinicalTrials.gov
For full trial details, please see the original record at
https://clinicaltrials.gov/study/NCT00352183
Registration number
NCT00352183
Ethics application status
Date submitted
13/07/2006
Date registered
14/07/2006
Date last updated
8/07/2009
Titles & IDs
Public title
Comparison of the Combination of Fenofibrate and 40 mg Simvastatin Versus 40 mg Simvastatin Monotherapy
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Scientific title
A Multicenter, Double-Blind, Randomized Study to Compare the Efficacy and Safety of the Combination of 145 mg Fenofibrate and 40 mg Simvastatin With 40 mg Simvastatin Monotherapy in Patients With Mixed Dyslipidemia at Risk of Cardiovascular Disease Not Adequately Controlled by 40 mg Simvastatin Alone.
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Secondary ID [1]
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ACTRN012605000777695
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Secondary ID [2]
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C LF0242780-01 05 02
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Universal Trial Number (UTN)
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Trial acronym
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Cardiovascular Diseases
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Condition category
Condition code
Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
Treatment: Drugs - Fenofibrate/Simvastatin
Treatment: Drugs - Simvastatin
Experimental: 1 -
Active comparator: 2 -
Treatment: Drugs: Fenofibrate/Simvastatin
Combination of Fenofibrate and Simvastatin 40mg
Treatment: Drugs: Simvastatin
Simvastatin 40mg
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Intervention code [1]
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Treatment: Drugs
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Comparator / control treatment
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Control group
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Outcomes
Primary outcome [1]
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Triglycerides
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Assessment method [1]
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Timepoint [1]
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12 weeks
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Primary outcome [2]
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Percent change from baseline to 12 weeks of treatment in HDL-C
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Assessment method [2]
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Timepoint [2]
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12 weeks
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Primary outcome [3]
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Percent change from baseline to 12 weeks of treatment in LDL-C
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Assessment method [3]
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Timepoint [3]
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12 weeks
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Secondary outcome [1]
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Percent change from baseline to 24 weeks of treatment in Triglycerides
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Assessment method [1]
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Timepoint [1]
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24 weeks
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Secondary outcome [2]
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Percent change from baseline to 24 weeks of treatment in HDL-C
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Assessment method [2]
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Timepoint [2]
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24 weeks
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Secondary outcome [3]
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Percent change from baseline to 24 weeks of treatment in LDL-C
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Assessment method [3]
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Timepoint [3]
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24 weeks
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Eligibility
Key inclusion criteria
* Mixed dyslipidemia
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Minimum age
18
Years
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Maximum age
75
Years
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Sex
Both males and females
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Can healthy volunteers participate?
No
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Key exclusion criteria
* Diabetes,
* Known hypersensitivity to fenofibrate or simvastatin,
* Pregnant or lactating women,
* Contra-indication to fenofibrate or simvastatin,
* Unstable or severe cardiac disease.
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Study design
Purpose of the study
Treatment
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Allocation to intervention
Randomised controlled trial
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Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
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Masking / blinding
Blinded (masking used)
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Who is / are masked / blinded?
The people receiving the treatment/s
The people analysing the results/data
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Intervention assignment
Parallel
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Other design features
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Phase
Phase 3
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Type of endpoint/s
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Statistical methods / analysis
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Recruitment
Recruitment status
Completed
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Data analysis
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Reason for early stopping/withdrawal
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Other reasons
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Date of first participant enrolment
Anticipated
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Actual
1/01/2006
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Date of last participant enrolment
Anticipated
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Actual
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Date of last data collection
Anticipated
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Actual
1/08/2008
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Sample size
Target
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Accrual to date
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Final
450
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Recruitment in Australia
Recruitment state(s)
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Recruitment hospital [1]
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Site 204 - Adelaide
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Recruitment hospital [2]
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Site 214 - Adelaide
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Recruitment hospital [3]
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Site 203 - Bendigo
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Recruitment hospital [4]
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Site 207 - Brisbane
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Recruitment hospital [5]
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Site 208 - Brisbane
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Recruitment hospital [6]
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Site 221 - Brisbane
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Recruitment hospital [7]
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Site 202 - Burnie
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Recruitment hospital [8]
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Site 201 - Camperdown
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Recruitment hospital [9]
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Site 220 - Coffs Harbour
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Recruitment hospital [10]
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Site 218 - Daw Park
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Recruitment hospital [11]
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Site 212 - Elizabeth Vale
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Recruitment hospital [12]
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Site 217 - Fitzroy
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Recruitment hospital [13]
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Site 222 - Fremantle
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Recruitment hospital [14]
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Site 216 - Geelong
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Recruitment hospital [15]
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Site 225 - Ingleburn
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Recruitment hospital [16]
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Site 213 - Kippa-ring
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Recruitment hospital [17]
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Site 209 - Launceston
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Recruitment hospital [18]
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Site 219 - Liverpool
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Recruitment hospital [19]
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Site 223 - Malvern
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Recruitment hospital [20]
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Site 211 - Meadowbrook
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Recruitment hospital [21]
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Site 224 - Miranda
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Recruitment hospital [22]
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Site 210 - Nambour
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Recruitment hospital [23]
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Site 205 - Parkville
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Recruitment hospital [24]
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Site 206 - Sale
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Recruitment hospital [25]
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Site 215 - Sydney
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Recruitment postcode(s) [1]
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- Adelaide
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Recruitment postcode(s) [2]
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- Bendigo
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Recruitment postcode(s) [3]
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- Brisbane
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Recruitment postcode(s) [4]
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- Burnie
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Recruitment postcode(s) [5]
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- Camperdown
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Recruitment postcode(s) [6]
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- Coffs Harbour
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Recruitment postcode(s) [7]
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- Daw Park
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Recruitment postcode(s) [8]
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- Elizabeth Vale
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Recruitment postcode(s) [9]
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- Fitzroy
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Recruitment postcode(s) [10]
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- Fremantle
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Recruitment postcode(s) [11]
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- Geelong
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Recruitment postcode(s) [12]
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- Ingleburn
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Recruitment postcode(s) [13]
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- Kippa-ring
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Recruitment postcode(s) [14]
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- Launceston
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Recruitment postcode(s) [15]
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- Liverpool
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Recruitment postcode(s) [16]
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- Malvern
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Recruitment postcode(s) [17]
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- Meadowbrook
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Recruitment postcode(s) [18]
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- Miranda
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Recruitment postcode(s) [19]
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- Nambour
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Recruitment postcode(s) [20]
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- Parkville
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Recruitment postcode(s) [21]
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- Sale
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Recruitment postcode(s) [22]
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- Sydney
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Recruitment outside Australia
Country [1]
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Estonia
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State/province [1]
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Tallinn
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Estonia
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State/province [2]
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Tartu
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Hungary
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Balatonfured
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Hungary
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Budapest
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Hungary
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Gyongyos
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Hungary
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Gyor
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Hungary
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Hodmezovasarhely
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Hungary
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Kecskemet
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Hungary
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Miskolc
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Hungary
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Sopron
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Hungary
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Szekesfehervar
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Latvia
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Daugavpils
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Latvia
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Jekabpils
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Latvia
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Ogre
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Latvia
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Riga
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Latvia
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Tukums
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Lithuania
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Alytus
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Lithuania
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Kaunas
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Lithuania
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Klaipeda
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Lithuania
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Palanga
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Lithuania
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Siauliai
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Lithuania
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Vilnius
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New Zealand
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Auckland
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New Zealand
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Blenheim
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New Zealand
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Christchurch
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New Zealand
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Dunedin
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New Zealand
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Hamilton
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New Zealand
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Hastings
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New Zealand
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Nelson
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New Zealand
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Newtown, Wellington
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New Zealand
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Takapuna, Auckland
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New Zealand
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State/province [32]
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Tauranga
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Funding & Sponsors
Primary sponsor type
Commercial sector/industry
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Name
Solvay Pharmaceuticals
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Address
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Country
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Ethics approval
Ethics application status
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Summary
Brief summary
Mixed or combined hyperlipidemia is a common metabolic disorder characterized by both hypercholesterolemia and hypertriglyceridemia. Statins and fibrates have complementary mechanisms and can be coadministered to patients with mixed hyperlipidemia. The overall objective of the study is to evaluate the efficacy and safety of combining fenofibrate and simvastatin in patients with mixed hyperlipidemia at risk of cardiovascular diseases.
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Trial website
https://clinicaltrials.gov/study/NCT00352183
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Trial related presentations / publications
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Public notes
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Contacts
Principal investigator
Name
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Global Clinical Director Solvay
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Address
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Solvay Pharmaceuticals
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Country
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Phone
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Fax
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Email
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Contact person for public queries
Name
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Address
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Country
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Phone
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Fax
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Email
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Contact person for scientific queries
No information has been provided regarding IPD availability
What supporting documents are/will be available?
No Supporting Document Provided
Results publications and other study-related documents
No documents have been uploaded by study researchers.
Results not provided in
https://clinicaltrials.gov/study/NCT00352183
Download to PDF