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Trial registered on ANZCTR
Registration number
ACTRN12605000519651
Ethics application status
Approved
Date submitted
12/09/2005
Date registered
26/09/2005
Date last updated
25/06/2008
Type of registration
Retrospectively registered
Titles & IDs
Public title
A Study to Determine the Linearity of the Pharmacokinetics and the Effect of Washing the Application Site on the Bioavailability of Estradiol from an Estradiol MDTS as hormone replacement therapy in post-menopausal women
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Scientific title
A Study to Determine the Linearity of the Pharmacokinetics and the Effect of Washing the Application Site on the Bioavailability of Estradiol from an Estradiol MDTS as hormone replacement therapy in post-menopausal women
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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:
Hormone replacement therapy in post-menopausal women
644
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Condition category
Condition code
Reproductive Health and Childbirth
717
717
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0
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Menstruation and menopause
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
Estradiol MDTS for 8 days
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Comparator / control treatment
No control
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Control group
Uncontrolled
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Outcomes
Primary outcome [1]
879
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Pharmacokinetic parameters
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Assessment method [1]
879
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Timepoint [1]
879
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On days 1 - 8
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Secondary outcome [1]
1743
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Safety and Tolerability
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Assessment method [1]
1743
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Timepoint [1]
1743
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Eligibility
Key inclusion criteria
Healthy post-menopausal women
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Minimum age
18
Years
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Maximum age
Not stated
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Sex
Females
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Can healthy volunteers participate?
Yes
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Key exclusion criteria
No exclusion criteria
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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)
None - Open label
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Computer generated in blocks
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Masking / blinding
Open (masking not used)
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Who is / are masked / blinded?
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Intervention assignment
Crossover
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Other design features
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Phase
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Type of endpoint/s
Pharmacokinetics
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Statistical methods / analysis
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Recruitment
Recruitment status
Completed
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Date of first participant enrolment
Anticipated
16/07/2001
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Actual
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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
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Sample size
Target
26
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Accrual to date
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Final
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Recruitment in Australia
Recruitment state(s)
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Funding & Sponsors
Funding source category [1]
793
0
Commercial sector/Industry
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Name [1]
793
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FemPharm Pty Ltd
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Address [1]
793
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Country [1]
793
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Australia
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Funding source category [2]
794
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Commercial sector/Industry
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Name [2]
794
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Acrux DDS Pty Ltd
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Address [2]
794
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Country [2]
794
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Australia
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Primary sponsor type
Commercial sector/Industry
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Name
FemPharm Pty Ltd and/or Acrux DDS Pty Ltd
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Address
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Country
Australia
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Secondary sponsor category [1]
657
0
None
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Name [1]
657
0
None
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Address [1]
657
0
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Country [1]
657
0
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Ethics approval
Ethics application status
Approved
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Summary
Brief summary
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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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Address
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Country
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Phone
35544
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Fax
35544
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Email
35544
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Contact person for public queries
Name
9688
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Karen Gard'ner
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Address
9688
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Acrux Drug Delivery Solutions (DDS) Pty Ltd
103-113 Stanley Street
West Melbourne VIC 3003
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Country
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Australia
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Phone
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+61 3 83790100
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Fax
9688
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Email
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[email protected]
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Contact person for scientific queries
Name
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Andrew Humberstone
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Address
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Acrux Drug Delivery Solutions (DDS) Pty Ltd
103-113 Stanley Street
West Melbourne VIC 3003
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Country
616
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Australia
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Phone
616
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+61 3 83790100
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Fax
616
0
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Email
616
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[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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