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Trial registered on ANZCTR
Registration number
ACTRN12606000329561
Ethics application status
Approved
Date submitted
4/07/2006
Date registered
3/08/2006
Date last updated
22/06/2016
Type of registration
Retrospectively registered
Titles & IDs
Public title
Sertraline Heart Study
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Scientific title
Efficacy of low dose Sertraline v's placebo in the amelioration of anxiety in heart disease.
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Universal Trial Number (UTN)
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Trial acronym
Nil
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Heart disease
1298
0
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Condition category
Condition code
Mental Health
1388
1388
0
0
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Anxiety
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Cardiovascular
1389
1389
0
0
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Coronary heart disease
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
Intervention 5mg Sertraline in a lactose base in an identical capsule. 1 d for 12/52 via oral route. The complete period of the trial is ~3 months.
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Intervention code [1]
1188
0
Treatment: Drugs
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Comparator / control treatment
Control: Lactose in an opaque capsule.
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Control group
Placebo
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Outcomes
Primary outcome [1]
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Reduction in anxiety
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Assessment method [1]
1892
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Timepoint [1]
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Measured at 6 weeks and again at 12 weeks
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Secondary outcome [1]
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Reduction in depression, reduction in fatigue, increase in effort tolerance and increase in quality of life.
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Assessment method [1]
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Timepoint [1]
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All will be measured at 6 and 12 weeks.
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Eligibility
Key inclusion criteria
Abnormal echocardiogram with history of any cardiac symptoms.
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Minimum age
18
Years
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Maximum age
85
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
Malignancy & Psychotrophics.
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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)
Allocation involved contacting the holder of the allocation schedule who was off-site
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Simple randomisation by using a randomisation table created by a computer based statistical program
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Masking / blinding
Blinded (masking used)
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Who is / are masked / blinded?
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Intervention assignment
Parallel
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Other design features
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Phase
Phase 4
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Type of endpoint/s
Efficacy
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Statistical methods / analysis
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Recruitment
Recruitment status
Stopped early
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Data analysis
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Reason for early stopping/withdrawal
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Date of first participant enrolment
Anticipated
1/01/2006
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Actual
1/01/2006
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Date of last participant enrolment
Anticipated
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Actual
1/07/2007
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Date of last data collection
Anticipated
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Actual
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Sample size
Target
100
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Accrual to date
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Final
1
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Recruitment in Australia
Recruitment state(s)
WA
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Recruitment hospital [1]
6010
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St John of God Hospital, Subiaco - Subiaco
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Recruitment postcode(s) [1]
13432
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6008 - Subiaco
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Funding & Sponsors
Funding source category [1]
1522
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Charities/Societies/Foundations
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Name [1]
1522
0
Mood Research Foundation (WA) Inc.
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Address [1]
1522
0
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Country [1]
1522
0
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Primary sponsor type
Charities/Societies/Foundations
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Name
Mood Research Foundation (WA) Inc
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Address
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Country
Australia
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Secondary sponsor category [1]
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None
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Name [1]
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Nil
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Address [1]
1337
0
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Country [1]
1337
0
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
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St John of God Hospital Subiaco Campus
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Ethics committee address [1]
2946
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Ethics committee country [1]
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Australia
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Date submitted for ethics approval [1]
2946
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Approval date [1]
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07/10/2004
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Ethics approval number [1]
2946
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132
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Summary
Brief summary
The low dose Sertraline Heart Study is a 3 month study evaluating improvements in energy, stress and well-being with very low dose Sertraline in patients with stable heart disease. Associated benefits may include improved sleep, weight and blood pressure. Being a serotonin reuptake inhibitor, we are also interested to monitor improvements in anxiety and mood, which have never been evaluated at this very low dose before. Half of the participants will receive 'blank' or placebo capsules. There are 4 visits to the study centre over the 3 months, at which symptoms will be monitored. Blood tests are undertaken initially and at 6 weeks. Subjects, Research Assistant and Medical Director are all blinded.
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Trial website
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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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Dr Simon Dimmitt
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Address
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c/o 3/10 McCourt St
WEST LEEDERVILLE WA 6007
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Country
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Australia
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Phone
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08 63809585
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Fax
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Email
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[email protected]
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Contact person for public queries
Name
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Dr Simon Dimmitt
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Address
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Suite 304/25
McCourt St
Subiaco WA 6008
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Country
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Australia
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Phone
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+61 8 93829580
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Fax
10377
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+61 8 93829586
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Email
10377
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[email protected]
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Contact person for scientific queries
Name
1305
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Dr Simon Dimmitt
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Address
1305
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Suite 304/25
McCourt St
Subiaco WA 6008
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Country
1305
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Australia
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Phone
1305
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+61 8 93829580
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Fax
1305
0
+61 8 93829586
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Email
1305
0
[email protected]
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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
Documents added manually
No documents have been uploaded by study researchers.
Documents added automatically
No additional documents have been identified.
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