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Trial registered on ANZCTR
Registration number
ACTRN12605000532606
Ethics application status
Approved
Date submitted
12/09/2005
Date registered
28/09/2005
Date last updated
28/09/2005
Type of registration
Retrospectively registered
Titles & IDs
Public title
How does raloxifene influence the effects of growth hormone replacement
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Scientific title
Modulation of growth hormone action during growth hormone replacement in growth hormone-deficient women: comparison of raloxifene and oral oestrogen
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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:
Hypopituitary women
657
0
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Condition category
Condition code
Metabolic and Endocrine
730
730
0
0
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Other metabolic and endocrine disorders
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
Raloxifene (60 mg daily) for 6 - 18 months
17 beta oestradiol (2 mg) for 6 - 18 months
recombinant uman growth hormone (Humaloge) (0.5 mg daily) for 24 months
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Intervention code [1]
526
0
None
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Comparator / control treatment
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Control group
Active
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Outcomes
Primary outcome [1]
900
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Short term measurements of biochemical markers of the GH-IGF-axis as well as substrate metabolism and protein turnover
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Assessment method [1]
900
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Timepoint [1]
900
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At baseline, after 1 month of growth hormone alone, growth hormone + raloxifene or growth hormone + oestradiol.
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Primary outcome [2]
901
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Long term effects on body composition measured by DEXA
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Assessment method [2]
901
0
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Timepoint [2]
901
0
At baseline, after 6 and 12 and 24 months.
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Secondary outcome [1]
1756
0
Changes in bone turnover markers and cardiovascular risk factors are measured:
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Assessment method [1]
1756
0
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Timepoint [1]
1756
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At baseline, after 1 month of growth hormone alone, growth hormone + raloxifene or growth hormone + oestradiol
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Secondary outcome [2]
1757
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Changes in bone turnover markers and cardiovascular risk factors are measured:
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Assessment method [2]
1757
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Timepoint [2]
1757
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On long term treatment with growth hormone + raloxifene or growth hormone + oestradiol after 6, 12 and 24 months.
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Secondary outcome [3]
1758
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Long term effects on body composition measured by DEXA.
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Assessment method [3]
1758
0
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Timepoint [3]
1758
0
At baseline, after 6 and 12 and 24 months.
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Eligibility
Key inclusion criteria
Hypopituitarism (deficient in growth hormone and sex steroids).
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Minimum age
Not stated
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Maximum age
Not stated
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Sex
Females
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Can healthy volunteers participate?
No
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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)
sealed envelopes
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
coin toss
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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
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
Active, not recruiting
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Date of first participant enrolment
Anticipated
5/09/2002
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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
12
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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]
811
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Government body
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Name [1]
811
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NHMRC
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Address [1]
811
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Country [1]
811
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Australia
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Primary sponsor type
Hospital
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Name
Department of Endocrinology, St Vincents Hospital Sydney
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Address
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Country
Australia
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Secondary sponsor category [1]
679
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None
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Name [1]
679
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none
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Address [1]
679
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Country [1]
679
0
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
2079
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Garvan Institute of Medical Research
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Ethics committee address [1]
2079
0
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Ethics committee country [1]
2079
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Australia
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Date submitted for ethics approval [1]
2079
0
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Approval date [1]
2079
0
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Ethics approval number [1]
2079
0
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Summary
Brief summary
Raloxifene is a member of a family of compounds called selective estrogen receptor modulators (SERMS) that exert many of the beneficial effects of estrogen replacement without the associated increase in risk of breast and uterine cancer. Growth hormone (GH) replacement is beneficial in adults with hypopituitarism. Most GH deficient women also require oestrogen replacement. Oral oestrogens antagonise GH action at the liver, thereby reducing its beneficial effects on body composition and metabolism. The aim of this study is to investigate whether SERMs exert less of a negative influence on the effects of GH replacement, and therefore would be superior to conventional estrogen replacement in this setting.
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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
35701
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Address
35701
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Country
35701
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Phone
35701
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Fax
35701
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Email
35701
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Contact person for public queries
Name
9715
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Dr Ken Ho
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Address
9715
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Professor of Medicine
Head
Pituitary Research Unit
Garvan Institute Chairman
Department of Endocrinology
Garvan Institute of Medical Research
St Vincents Hospital
384 Victoria Street
Darlinghurst NSW 2010
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Country
9715
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Australia
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Phone
9715
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+61 2 92958203
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Fax
9715
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+61 2 92958411
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Email
9715
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[email protected]
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Contact person for scientific queries
Name
643
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Dr Udo Meinhardt
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Address
643
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Pituitary Research Unit
Garvan Institute of Medical Research
384 Victoria St
Darlinghurst NSW 2010
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Country
643
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Australia
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Phone
643
0
+61 2 92958486
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Fax
643
0
+61 2 92958411
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Email
643
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
Source
Title
Year of Publication
DOI
Dimensions AI
Effects of raloxifene and estrogen on bioactive IGF1 in GH-deficient women
2014
https://doi.org/10.1530/eje-13-0835
N.B. These documents automatically identified may not have been verified by the study sponsor.
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