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Trial registered on ANZCTR
Registration number
ACTRN12610000265077
Ethics application status
Not yet submitted
Date submitted
29/03/2010
Date registered
31/03/2010
Date last updated
31/03/2010
Type of registration
Prospectively registered
Titles & IDs
Public title
The sustained effects of Osteopathic Treatment on Primary Dysmennorhoea
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Scientific title
In patients with primary dysmennorhoea, is sustained osteopathic treatment more beneficial than medication in reducing pain and medication usage?
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Secondary ID [1]
1528
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None
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Universal Trial Number (UTN)
U1111-1114-5008
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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:
Primary dysmennorhoea
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Condition category
Condition code
Reproductive Health and Childbirth
257165
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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
Osteopathic treatment. The osteopathic treatments are conducted at the Victoria University Teaching Clinic with consultations approximately 45 minutes in duration. Treatment will be administered twice per week during the fortnight before menstruation. Treatment will continue over two months (four treatment consultations in total) with the last two months being used to determine if there is a long term effect of osteopathic treatment.
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Intervention code [1]
256182
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Treatment: Other
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Comparator / control treatment
allopathic medication. Patients will not be administered any medication. Patients will be instructed to continue the use of allopathic medication as they would normally.
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Control group
Active
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Outcomes
Primary outcome [1]
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Pain scales. We will use the Mankoski Pain Scale. This is a functional pain scale particularly concerned with period pain. Patients are asked to rate their level of pain on a scale of 0-10 (0= pain free, with 10 = unconcious due to the pain). Our patients will be required to suffer from Period pain of a level of 3 = annoying enough to be distracting in order to determine any effects of osteopathic treatment.
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Assessment method [1]
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Timepoint [1]
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pre-commencement baseline, then monthly for four months
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Secondary outcome [1]
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medication diary for medication usage
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Assessment method [1]
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Timepoint [1]
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pre-commencement baseline, then monthly for four months
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Eligibility
Key inclusion criteria
Patients suffering from primary dysmennorhoea with no pathological cause
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Minimum age
18
Years
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Maximum age
40
Years
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Sex
Females
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Can healthy volunteers participate?
No
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Key exclusion criteria
Participants suffering from secondary dysmennorhoea, outside age range, or pregnant
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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)
Subjects sought via advertising in university teaching clinic and email to staff and students of the university. We will use numbered containers for allocation concealment
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Numbers out of a hat
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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
Parallel
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Other design features
use of pre-trial medication diaries to establish medication baseline
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Phase
Not Applicable
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Type of endpoint/s
Efficacy
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Statistical methods / analysis
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Recruitment
Recruitment status
Not yet recruiting
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Date of first participant enrolment
Anticipated
1/04/2010
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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
20
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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]
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Self funded/Unfunded
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Name [1]
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Address [1]
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Country [1]
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Australia
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Primary sponsor type
Individual
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Name
Dr. Brian Nicholls
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Address
Victoria University,
301 Flinders Lane,
Melbourne, Vic. 3000
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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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Address [1]
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Country [1]
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Ethics approval
Ethics application status
Not yet submitted
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Ethics committee name [1]
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Victoria University Human Research Ethics Commitee
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Ethics committee address [1]
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Victoria University Footscray Park Campus Ballarat road Footscray VIC, 3011
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Ethics committee country [1]
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Australia
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Date submitted for ethics approval [1]
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11/02/2010
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Approval date [1]
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Ethics approval number [1]
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HRETH 09/190
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Summary
Brief summary
A randomised controlled intervention study investigating the effect of sustained osteopathic treatment on the pain levels and medication usage in primary dysmennorrhoea
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Trial website
none
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Trial related presentations / publications
none
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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
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Fax
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Email
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Contact person for public queries
Name
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Dr Brian Nicholls
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Address
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Victoria University
Flinders Lane Campus
Level 4, 301 Flinders Lane
Melbourne
VIC 3000
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Country
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Australia
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Phone
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+61 3 99191150
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Fax
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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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Dr Brian Nicholls
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Address
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Victoria University
Flinders Lane Campus
Level 4, 301 Flinders Lane
Melbourne
VIC 3000
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Country
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Australia
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Phone
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+61 3 99191150
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Fax
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Email
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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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