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Trial registered on ANZCTR
Registration number
ACTRN12611000984998
Ethics application status
Approved
Date submitted
12/09/2011
Date registered
15/09/2011
Date last updated
25/06/2019
Date data sharing statement initially provided
25/06/2019
Type of registration
Prospectively registered
Titles & IDs
Public title
PRP (Autologous Platelet rich plasma) may improve hip arthroscopy patients outcome.
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Scientific title
In patients undergoing hip arthroscopy, how would platelet rich plasma, compared with placebo, improve post operative outcome in the short and long term.
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Secondary ID [1]
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Nil
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Universal Trial Number (UTN)
U1111-1124-5099
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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:
The study Will include patients who elect to go through a surgical procedure in order to treat a pre existing hip injury such as FAI (Femoral acetabular impingement).
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Condition category
Condition code
Musculoskeletal
270940
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0
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Other muscular and skeletal disorders
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Surgery
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0
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Other surgery
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
The treatment group would be treated with platelets concentrate prepared from their own blood (which was drown by 4 regular 5 cc blood collecting tubes). The concentrate will be applied to the operated area (hip) 24 hours after the surgery via a drainage left
at the site during the procedure.
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Intervention code [1]
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Treatment: Other
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Comparator / control treatment
Placebo group will go through the same process as above without applying the PRP concentrate into the joint. instead the same volume of saline would be administrated.
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Control group
Placebo
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Outcomes
Primary outcome [1]
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Suffer from less surgical known side effects such as long term incidental pain or activity restrictions.
MAHORN validated questioner.
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Assessment method [1]
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Timepoint [1]
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1,3,6,12 months
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Secondary outcome [1]
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To have a better cartilage and labral healing as seen on MRI
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Assessment method [1]
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Timepoint [1]
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6, 12 month
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Eligibility
Key inclusion criteria
1. healthy patients undergoing hip Arthroscopy due to FAI
2. Ages 16-50
3. No OA changes according to XR and surgery observation
4. No previous hip surgery
5. No other influential disabilities in lower limbs 6. No chronic use of NSAID, steroids or chemotherapy drugs
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Minimum age
16
Years
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Maximum age
50
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
Non-ambulating patients, those with severe advanced osteoarthritic changes on radiological imaging, patients with suspected previous joint infection, pregnant or lactating women, open wounds or skin ulcers and those taking anticoagulants or having a prolonged bleeding time were excluded.
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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)
Allocation was concealed using numbered containers
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Simple randomisation using a randomisation table created by computer software
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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
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
Completed
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Date of first participant enrolment
Anticipated
20/09/2011
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Actual
20/09/2011
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Date of last participant enrolment
Anticipated
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Actual
29/06/2012
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Date of last data collection
Anticipated
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Actual
21/06/2019
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Sample size
Target
100
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Accrual to date
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Final
105
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Recruitment outside Australia
Country [1]
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New Zealand
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State/province [1]
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AUCKLAND
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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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Dr. Omer Mei-Dan
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Address [1]
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27 Prospect Terrace, Milford
0620
Auckland
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Country [1]
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New Zealand
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Primary sponsor type
Individual
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Name
Dr. Omer Mei-Dan
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Address
27 Prospect Terrace, Milford
0620
Auckland
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Country
New Zealand
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Secondary sponsor category [1]
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Individual
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Name [1]
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Dr. Mat Brick
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Address [1]
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Millennium Institute of Sport and Health
17 Antares Place
Mairangi Bay
North Shore City, Auckland
0632
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Country [1]
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New Zealand
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
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Northern Y Regional Ethics Committee
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Ethics committee address [1]
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Ministry of health, 3rd floor, BNZ building, 354 Victoria st. PO Box 1031 Hamilton 3204
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Ethics committee country [1]
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New Zealand
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Date submitted for ethics approval [1]
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01/03/2011
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Approval date [1]
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09/08/2011
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Ethics approval number [1]
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NTY/11/04/043
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Summary
Brief summary
Hip arthroscopy is a surgical treatment technique which commonly address intra articular cartilage and labral pathologies. There is a growing evidence that PRP can improve articular cartilage healing, both when applied during surgery or as a sole method of treatment, when prescribed for the proper indication. PRP injection has been proposed as a novel treatment modality for the management of articular cartilage injuries of the knee, hip and ankle. Even though high level of clinical evidence is lacking, basic research supports the use of PRP derived growth factors to improve tissue healing. There are few published clinical studies on the use of PRP in cartilage pathology. The study hypothesis is that the new treatment (PRP) would improve patients outcome after arthroscopic treatment for FAI (hip impingement).
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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 Joshua Knudsen
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Address
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Orthosports
17 Antares Pl, Rosedale, Auckland 0632
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Country
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New Zealand
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Phone
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+64 212011130
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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. Omer Mei-Dan
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Address
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Millennium Institute of Sport and Health
17 Antares Place
Mairangi Bay
North Shore City, Auckland
0632
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Country
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New Zealand
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Phone
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0064 9 477 2080
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Fax
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0064 9 477 2091
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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. Omer Mei-Dan
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Address
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Millennium Institute of Sport and Health
17 Antares Place
Mairangi Bay
North Shore City, Auckland
0632
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Country
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New Zealand
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Phone
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0064 21 883839
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Fax
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0064 9 477 2091
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Email
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[email protected]
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Data sharing statement
Will individual participant data (IPD) for this trial be available (including data dictionaries)?
No
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No/undecided IPD sharing reason/comment
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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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