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Trial registered on ANZCTR
Registration number
ACTRN12612000982819
Ethics application status
Approved
Date submitted
10/09/2012
Date registered
12/09/2012
Date last updated
17/07/2018
Type of registration
Prospectively registered
Titles & IDs
Public title
Northland Lateral Hip Pain Platelet-Rich Plasma Treatment Study
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Scientific title
Northland, New Zealand Musculoskeletal Group Study on the effectiveness of Platelet-Rich Plasma for the treatment of Greater Trochanteric Pain Syndrome.
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Secondary ID [1]
281205
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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:
Chronic Greater Trochanteric Pain Syndrome
287382
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Condition category
Condition code
Musculoskeletal
287715
287715
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0
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Other muscular and skeletal disorders
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
60 millilitres of blood will be drawn from the participant, and this will be immediately centrifuged to produce 5-6 millilitres of platelet-rich plasma which will be then given with local anaesthetic as a single once-off injection into the focal area of pain and tenderness over the outer hip. The process from taking the blood to doing the injection should be under 20 minutes.
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Intervention code [1]
285669
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Treatment: Other
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Comparator / control treatment
Placebo (Saline & Local Anaesthetic)
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Control group
Placebo
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Outcomes
Primary outcome [1]
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Change in reported pain intensity (measured as change in pain score on a Numeric Rating Scale (NCS) from baseline.
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Assessment method [1]
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Timepoint [1]
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6 months
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Secondary outcome [1]
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Function (using Brief Pain Inventory)
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Assessment method [1]
299144
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Timepoint [1]
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6 months
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Secondary outcome [2]
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Sleep (using BPI)
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Assessment method [2]
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Timepoint [2]
299145
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6 months
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Secondary outcome [3]
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Utilisation of Health Resources (Consultations, Medication Use, other interventions) using participant recall.
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Assessment method [3]
299146
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Timepoint [3]
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6 months
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Eligibility
Key inclusion criteria
Spontaneous pain in the lateral aspect of the hip
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Minimum age
18
Years
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Maximum age
70
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
Serious medical or psychologic disorders, History of operation in the same area, Anti-coagulants, Pregnancy, High performance athletes, Low haemoglobin or platelet count, inability to understand questionnaires.
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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)
Computer generated randomisation, concealment by use of coded identifier for intervention.
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Computer generated.
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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
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Type of endpoint/s
Efficacy
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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
1/01/2013
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Actual
15/02/2013
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Date of last participant enrolment
Anticipated
12/04/2013
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Actual
12/04/2013
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Date of last data collection
Anticipated
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Actual
16/07/2018
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Sample size
Target
48
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Accrual to date
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Final
48
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Recruitment outside Australia
Country [1]
4546
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New Zealand
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State/province [1]
4546
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Northland
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Funding & Sponsors
Funding source category [1]
285984
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Self funded/Unfunded
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Name [1]
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Dr Grant Thompson
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Address [1]
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PO Box 4274
Kamo
Whangarei 0141
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Country [1]
285984
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New Zealand
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Primary sponsor type
Individual
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Name
Dr Grant Thompson
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Address
PO Box 4274
Kamo
Whaangarei 0141
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Country
New Zealand
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Secondary sponsor category [1]
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None
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Name [1]
284802
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Address [1]
284802
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Country [1]
284802
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
288018
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Northern B Health and Disability Ethics Committee
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Ethics committee address [1]
288018
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Ministry of Health PO Box 5013 Wellington 6011
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Ethics committee country [1]
288018
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New Zealand
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Date submitted for ethics approval [1]
288018
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01/10/2012
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Approval date [1]
288018
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20/12/2012
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Ethics approval number [1]
288018
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Summary
Brief summary
Double blinded randomised comparison of single injection of Platelet-Rich Plasma for the treatment of Greater Trochanteric Pain Syndrome.
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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 Grant Thompson
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Address
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PO Box 4274
Kamo
Whangarei
New Zealand 0141
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Country
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New Zealand
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Phone
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+64 9 4594400
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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 Grant Thompson
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Address
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PO Box 4724
Kamo
Whangarei 0141
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Country
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New Zealand
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Phone
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+64 9 459 4400
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Fax
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+64 9 459 4455
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Email
17942
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[email protected]
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Contact person for scientific queries
Name
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Dr Grant Thompson
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Address
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PO Box 4274
Kamo
Whangarei 0141
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Country
8870
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New Zealand
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Phone
8870
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+64 9 459 4400
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Fax
8870
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+64 9 459 4455
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Email
8870
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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
Source
Title
Year of Publication
DOI
Embase
Platelet-rich therapies for musculoskeletal soft tissue injuries.
2013
https://dx.doi.org/10.1002/14651858.CD010071.pub2
N.B. These documents automatically identified may not have been verified by the study sponsor.
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