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Trial registered on ANZCTR
Registration number
ACTRN12615001193561
Ethics application status
Approved
Date submitted
17/09/2015
Date registered
4/11/2015
Date last updated
7/10/2021
Date data sharing statement initially provided
7/10/2021
Type of registration
Prospectively registered
Titles & IDs
Public title
A pilot study of dose schedules for pamidronate infusions in the management of non-specific low back pain
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Scientific title
A pilot study comparing two dose schedules(two 90 mg doses on consecutive days versus two 90mg doses 28 days apart) for the delivery of intravenous pamidronate in the management of chronic non-specific low back pain.
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Secondary ID [1]
287491
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none
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Universal Trial Number (UTN)
U1111-1170-4165
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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:
non-specific Low back Pain
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Condition category
Condition code
Anaesthesiology
296506
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0
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Pain management
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Musculoskeletal
296898
296898
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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
Pamidronate infusion of 90mg.
Two doses given either on consecutive days or 28 days apart.
Each dose given over 4 hours in hospital ward.
Infusion monitored by study nurse or doctor.
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Intervention code [1]
292874
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Treatment: Drugs
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Comparator / control treatment
Comparison of dose schedules of pamidronate in non specific low back pain.
Comparison of two 90 mg doses given on consecutive days and 28 days apart.
The dose given 28 days apart is the control dose.
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Control group
Active
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Outcomes
Primary outcome [1]
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Proportion of patients who show an improvement in Pain Scores measured on the Brief Pain Inventory (short form)
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Assessment method [1]
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Timepoint [1]
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90 days post infusion- primary time point
180 days post infusion- secondary time point- completion of study
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Secondary outcome [1]
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Global impression of change(Quality of life)
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Assessment method [1]
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Timepoint [1]
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six months post first infusion dose
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Eligibility
Key inclusion criteria
Patients referred to chronic pain clinic at Tauranga Hospital.
Chronic non specific low back pain of at least three months duration
Pain score greater than 4 on numerical rating scale
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Minimum age
18
Years
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Maximum age
No limit
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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
Primary diagnosis of radicular or neuropathic pain
Vertebral compression fracture or cancer
Allergy to pamidronate
Significant other medical problems (renal, liver, cardiac, respiratory)
History of alcohol or drug abuse
Pending legal or compensation claim
Planned surgery or significant intervention in next six months
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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
Parallel
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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
Completed
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Date of first participant enrolment
Anticipated
16/11/2015
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Actual
16/03/2016
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Date of last participant enrolment
Anticipated
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Actual
14/10/2019
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Date of last data collection
Anticipated
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Actual
17/03/2020
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Sample size
Target
40
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Accrual to date
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Final
40
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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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Bay Of Plenty
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Funding & Sponsors
Funding source category [1]
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Charities/Societies/Foundations
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Name [1]
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BOP Medical Research Trust
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Address [1]
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BOP Medical Research Trust
PO Box 752
Tauranga 3140
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Country [1]
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New Zealand
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Primary sponsor type
Hospital
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Name
Tauranga Hospital. Bay Of Plenty DHB
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Address
Tauranga Hospital
Cameron Road
Private Bag 12024
Tauranga 3143
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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]
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Address [1]
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Country [1]
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
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Health and Disability ethics comittee. Northern B
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Ethics committee address [1]
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Ministry of Health Ethics Department Freyberg Building Reception – Ground Floor 20 Aitken Street Wellington 6011 .
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Ethics committee country [1]
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New Zealand
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Date submitted for ethics approval [1]
293550
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Approval date [1]
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11/08/2015
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Ethics approval number [1]
293550
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15\MTB\130
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Summary
Brief summary
A randomized cohort pilot trial which will compare any significant statistical differences in either benefit or adverse effects on participants pain scores and quality of life when given a Pamidronate infusion(total dose 180mg) either on two consecutive days or 28 days apart to aid in the management of chronic non-specific low back pain.
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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 Saad Anis
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Address
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Chronic Pain Service
Tauranga Hospital
Private Bag 12024
Tauranga
3143
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Country
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New Zealand
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Phone
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+64 7 557 5038
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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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Vicky Beveridge
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Address
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Chronic Pain Service
Tauranga Hospital
Private Bag 12024
Tauranga
3143
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Country
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New Zealand
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Phone
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+64 7 557 5038
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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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Saad Anis
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Address
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Chronic Pain Service
Tauranga Hospital
Private Bag 12024
Tauranga
3143
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Country
57476
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New Zealand
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Phone
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+64 7 557 5038
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Fax
57476
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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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