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Trial details imported from ClinicalTrials.gov
For full trial details, please see the original record at
https://clinicaltrials.gov/study/NCT05422248
Registration number
NCT05422248
Ethics application status
Date submitted
13/06/2022
Date registered
16/06/2022
Date last updated
13/09/2023
Titles & IDs
Public title
Oxygen Wound Therapy Feasibility Study
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Scientific title
Oxygen Wound Therapy Feasibility Study
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Secondary ID [1]
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CIA-297
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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 Leg Ulcer
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Condition category
Condition code
Skin
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Other skin conditions
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Cardiovascular
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Diseases of the vasculature and circulation including the lymphatic system
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
Treatment: Devices - Series Topical Oxygen Therapy
Treatment: Devices - Paired Topical Oxygen Therapy
Active comparator: Series - Standard wound care for 4 weeks followed by intervention device wound care for up to 12 weeks.
Active comparator: Paired - Intervention device wound care to a portion of wound and standard wound care to the remaining portion of the wound, for up to 12 weeks.
Treatment: Devices: Series Topical Oxygen Therapy
Standard care provided to the whole wound followed by intervention device care to the whole wound.
Treatment: Devices: Paired Topical Oxygen Therapy
Care provided to one portion of wound by intervention device and standard care to remaining portion of wound.
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Intervention code [1]
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Treatment: Devices
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Comparator / control treatment
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Control group
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Outcomes
Primary outcome [1]
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Change in wound area
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Assessment method [1]
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cm\^2
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Timepoint [1]
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12 weeks
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Eligibility
Key inclusion criteria
* Patients with hard to heal lower leg wounds as determined by the treating clinician.
* Patient has a wound area greater than the area of the interface
* Aged 16 years and over
* Able to provide informed consent
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Minimum age
16
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
* Lower limb wounds with bone or tendon exposed
* Infected wounds which require treatment with antibiotics
* Wounds with critical bioburden requiring a medicated dressing
* Wounds that require dressing changes more than every second day, for example high exudating wounds
* Wounds with slough covering more than 30% of the wound surface
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Study design
Purpose of the study
Treatment
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Allocation to intervention
Non-randomised 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
NA
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Type of endpoint/s
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Statistical methods / analysis
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Recruitment
Recruitment status
Recruiting
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Data analysis
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Reason for early stopping/withdrawal
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Other reasons
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Date of first participant enrolment
Anticipated
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Actual
1/12/2022
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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
1/08/2026
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Actual
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Sample size
Target
10
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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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Recruitment outside Australia
Country [1]
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New Zealand
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State/province [1]
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Otago
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Funding & Sponsors
Primary sponsor type
Commercial sector/industry
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Name
Fisher and Paykel Healthcare
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Address
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Country
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Ethics approval
Ethics application status
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Summary
Brief summary
Determine the feasibility of using a new topical oxygen therapy device to treat hard to heal lower leg wounds.
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Trial website
https://clinicaltrials.gov/study/NCT05422248
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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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Jolanta Krysa
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Address
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Southern DHB Vascular Surgery
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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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Geoff Bold
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Address
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Country
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Phone
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+64 (09) 574 0100
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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
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
No documents have been uploaded by study researchers.
Results not provided in
https://clinicaltrials.gov/study/NCT05422248
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