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Trial registered on ANZCTR
Registration number
ACTRN12610000343000
Ethics application status
Not yet submitted
Date submitted
8/04/2010
Date registered
29/04/2010
Date last updated
29/04/2010
Type of registration
Prospectively registered
Titles & IDs
Public title
Effect of abdominoplasty on quality of life and self esteem
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Scientific title
In patients having had abdominoplasty is there a difference in post vs. presurgical qualilty of life and self esteem
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Secondary ID [1]
1611
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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:
Quality of Life in Abdominoplasty patients
257189
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Condition category
Condition code
Surgery
257333
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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
A standard abdominplasty procedure is performed in general anaesthesia. The operation may include liposuction. Skin and subcutaneous tissue between the umbilical level and and the pubic region is incised and removed. The upper skin flap is centrally undermined and sutured to the caudal wound edge. The procedure takes approx. 2 h. The procedure is a one-off treatment.
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Intervention code [1]
241189
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Treatment: Surgery
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Comparator / control treatment
Preoperative condition
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Control group
Uncontrolled
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Outcomes
Primary outcome [1]
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Quality of life measured by Short Form 36 (SF-36), Derriford Appearance Scale 24 (DAS24) and Multidimensional Body Self Relations Questionnaire (MBSRQ)
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Assessment method [1]
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Timepoint [1]
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Each patient is asked to participate in a single study consultation 6-24 months post operatively.
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Primary outcome [2]
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Visual (based on standardized photos) evaluation of operative result
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Assessment method [2]
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Timepoint [2]
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Photos are taken at Timepoint 1 (no extra consultation).
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Secondary outcome [1]
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nil
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Assessment method [1]
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Timepoint [1]
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nil
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Eligibility
Key inclusion criteria
Abdominoplasty patients operated at our
department
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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
Body Mass Index (BMI) >33
Large hernias
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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)
75 consequitive patiens who have had abdominoplasty at our department will be sent an invitation to participate in the study. These patient have been offered public funded abdominoplasty due to gross abdominal skin surplus and ailments like intertrigo, pain and infection.
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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
Single group
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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
Not yet recruiting
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Date of first participant enrolment
Anticipated
1/06/2010
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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
75
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Accrual to date
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Final
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Recruitment outside Australia
Country [1]
1963
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Norway
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State/province [1]
1963
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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]
256784
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Country [1]
256784
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Norway
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Primary sponsor type
Individual
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Name
Bjorn M. Hokland
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Address
Bjorn M. Hokland, MD, PhD, Dept Plastic and Reconstructive Surgery, Oslo University Hospital, Ulleval, 0407 Oslo
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Country
Norway
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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]
256060
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Country [1]
256060
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Ethics approval
Ethics application status
Not yet submitted
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Ethics committee name [1]
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Regional Ethics Commitee South East
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Ethics committee address [1]
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Post Box 1130 Blindern, 0318 Oslo, Norway
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Ethics committee country [1]
258807
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Norway
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Date submitted for ethics approval [1]
258807
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08/04/2010
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Approval date [1]
258807
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Ethics approval number [1]
258807
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Summary
Brief summary
In Norway patients may be offered publicly funded abdominoplasty when there is a large skin overhang combined with severe skin infection. The aim of the study is to investigate the effect of operative treatment on Quality of Life and self esteem.
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Trial website
No trial wesite.
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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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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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Bjorn M. Hokland
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Address
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Dept Plast Rec Surgery, Oslo University Hospital, Ulleval, 0407 Oslo, Norway
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Country
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Norway
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Phone
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0047 22 11 80 80
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Fax
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0047 22 11 95 58
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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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Bjorn M. Hokland
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Address
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Dept Plast Rec Surgery, Oslo University Hospital, Ulleval, 0407 Oslo, Norway
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Country
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Norway
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Phone
4270
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0047 22 11 80 80
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Fax
4270
0
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Email
4270
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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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