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Trial registered on ANZCTR
Registration number
ACTRN12616000114448
Ethics application status
Approved
Date submitted
31/08/2015
Date registered
2/02/2016
Date last updated
17/07/2018
Type of registration
Prospectively registered
Titles & IDs
Public title
a study for dosage of Andriol Testocaps in treatment of late-onset hypogonadism
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Scientific title
differential dosage of Andriol Testocaps in treatment of Chinese patients with late-onset hypogonadism
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Secondary ID [1]
287252
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nil
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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:
late-onset hypogonadism
295867
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Condition category
Condition code
Reproductive Health and Childbirth
296115
296115
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0
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Other reproductive health and childbirth disorders
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Metabolic and Endocrine
297014
297014
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0
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Other metabolic disorders
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
lower dosage of Testosterone Undecanoate Capsule (Andriol) as two groups (40mg and 80mg orally. daily) for 12 weeks and monitored by drug tablet return
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Intervention code [1]
292546
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Treatment: Drugs
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Comparator / control treatment
routine dosage(80mg orally per 12 hours) for 12 weeks
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Control group
Dose comparison
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Outcomes
Primary outcome [1]
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change in testosterone level with serum assay
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Assessment method [1]
295982
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Timepoint [1]
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three months post randomisation
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Secondary outcome [1]
317091
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proportion of participants with an improvement of LOH syndrome by Androgen Deficiency in the Aging Male questionnaire (ADAM)
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Assessment method [1]
317091
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Timepoint [1]
317091
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three months post randomisation
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Eligibility
Key inclusion criteria
Inclusion criteria:
1. serum testerone level <350ng/dl
2.decreased sexual desire
3. erection dysfunctiond
participants with all the 3 criteria together should be eligible
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Minimum age
30
Years
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Maximum age
70
Years
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Sex
Males
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Can healthy volunteers participate?
No
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Key exclusion criteria
1.abnormal PSA or prostate cancer
2.hematocrit>45%
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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
Open (masking not used)
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Who is / are masked / blinded?
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Intervention assignment
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Other design features
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Phase
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Type of endpoint/s
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Statistical methods / analysis
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Recruitment
Recruitment status
Withdrawn
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Reason for early stopping/withdrawal
Lack of funding/staff/facilities
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Date of first participant enrolment
Anticipated
12/02/2016
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Actual
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Date of last participant enrolment
Anticipated
1/12/2016
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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
60
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Accrual to date
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Final
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Recruitment outside Australia
Country [1]
7128
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China
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State/province [1]
7128
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shanghai
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Funding & Sponsors
Funding source category [1]
291940
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Self funded/Unfunded
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Name [1]
291940
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unfunded
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Address [1]
291940
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unfunded
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Country [1]
291940
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Primary sponsor type
Individual
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Name
zhou tie
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Address
shanghai changhai road 168#, shanghai changhai hospital., shanghai, China, 200433
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Country
China
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Secondary sponsor category [1]
290610
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None
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Name [1]
290610
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Address [1]
290610
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Country [1]
290610
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
293860
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changhai hospital ethics committee
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Ethics committee address [1]
293860
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shanghai changhai road 168#, shanghai changhai hospital., shanghai, China, 200433
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Ethics committee country [1]
293860
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China
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Date submitted for ethics approval [1]
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02/09/2015
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Approval date [1]
293860
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12/10/2015
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Ethics approval number [1]
293860
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Summary
Brief summary
Overload dosage of Andriol Testocaps will not benefit the patients with LOH. In China, the patients with LOH were administrated with same dosage of Andriol Testocaps but lower BMI or weight compared with the westerns. Obviously, drug dosage heavily depends on the weight and BMI. Thus if Chinese patients are given similar dosage of Andriol Testocaps to the western patients, they may face the overdosage of Andriol Testocaps. In this study, we investigate the appropriate dosage of Andriol Testocaps for Chinese patients with LOH.
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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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Prof zhou tie
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Address
59426
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shanghai changhai road 168#, shanghai changhai hospital., shanghai, China, 200433
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Country
59426
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China
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Phone
59426
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+8613918360523
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Fax
59426
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Email
59426
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[email protected]
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Contact person for public queries
Name
59427
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zhou tie
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Address
59427
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shanghai changhai road 168#, shanghai changhai hospital., shanghai, China, 200433
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Country
59427
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China
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Phone
59427
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+8613918360523
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Fax
59427
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Email
59427
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[email protected]
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Contact person for scientific queries
Name
59428
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zhou tie
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Address
59428
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shanghai changhai road 168#, shanghai changhai hospital., shanghai, China, 200433
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Country
59428
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China
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Phone
59428
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+8613918360523
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Fax
59428
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Email
59428
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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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