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Trial details imported from ClinicalTrials.gov
For full trial details, please see the original record at
https://clinicaltrials.gov/study/NCT00484835
Registration number
NCT00484835
Ethics application status
Date submitted
8/06/2007
Date registered
11/06/2007
Date last updated
8/08/2007
Titles & IDs
Public title
Are Sutures Required in Total Abdominal Hysterectomy? A Randomised Control Trial
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Scientific title
Randomised Control Trial Comparing Hysterectomy Using Electrocoagulation Forceps With the Traditional Clamp & Suture Technique of Richardson Abdominal Hysterectomy
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Secondary ID [1]
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Electrocoag Forceps in TAH
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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:
Total Abdominal Hysterectomy
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Condition category
Condition code
Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
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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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Operating time, Blood loss, Post-operative pain
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Assessment method [1]
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Timepoint [1]
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1 year
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Secondary outcome [1]
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Length of hospital stay, Cost of the procedure
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Assessment method [1]
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Timepoint [1]
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1 year
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Eligibility
Key inclusion criteria
* Any patient already on waitlist in Southern Health for abdominal hysterectomy with suspected benign pathology
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Minimum age
No limit
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Maximum age
No limit
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Sex
Females
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Can healthy volunteers participate?
Yes
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Key exclusion criteria
* Patients without consent and/or with suspected malignant pathology
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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 1
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Type of endpoint/s
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Statistical methods / analysis
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Recruitment
Recruitment status
UNKNOWN
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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
1/09/2007
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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
1/08/2008
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Actual
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Sample size
Target
60
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Accrual to date
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Final
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Recruitment in Australia
Recruitment state(s)
VIC
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Recruitment hospital [1]
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Casey Hospital - Melbourne
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Recruitment hospital [2]
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Dandenong Hospital - Melbourne
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Recruitment hospital [3]
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Monash Medical Centre(Moorabin) - Melbourne
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Recruitment postcode(s) [1]
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- Melbourne
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Funding & Sponsors
Primary sponsor type
Other
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Name
Southern Health
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Address
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Country
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Other collaborator category [1]
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Commercial sector/industry
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Name [1]
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Gyrus ACMI
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Address [1]
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Country [1]
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Ethics approval
Ethics application status
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Summary
Brief summary
The Hypothesis of this study is that performing total abdominal hysterectomy using the newer electrocoagulation forceps, specifically, the gyrus open seal forceps, curved, compared to the traditional clamp \& suture technique will result in reduction of operating time, intra-operative blood loss, post-operative pain.
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Trial website
https://clinicaltrials.gov/study/NCT00484835
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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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Marziya Kadir, MBBS
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Address
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Southern Health
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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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Marziya Kadir, MBBS
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Address
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Country
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Phone
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613 95946666
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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/NCT00484835
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