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Trial registered on ANZCTR
Registration number
ACTRN12605000217606
Ethics application status
Approved
Date submitted
23/08/2005
Date registered
26/08/2005
Date last updated
26/08/2005
Type of registration
Retrospectively registered
Titles & IDs
Public title
A prospective, randomized, double-blind, placebo-controlled trial of multimodal intraoperative analgesia for laparoscopic excision of endometriosis.
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Scientific title
A prospective, randomized, double-blind, placebo-controlled trial of the efficacy of multimodal intraoperative analgesia on post-operative pain levels and analgesia requirements on laparoscopic excision of endometriosis.
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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:
Laparoscopic surgery and endometriosis
300
0
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Condition category
Condition code
Reproductive Health and Childbirth
341
341
0
0
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Other reproductive health and childbirth disorders
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Surgery
342
342
0
0
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Other surgery
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Anaesthesiology
343
343
0
0
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Other anaesthesiology
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
Multimodal analgesia
(Diclofenac sodium 100mg suppository PR, 0.75% Ropivacaine)
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Intervention code [1]
234
0
Treatment: Drugs
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Comparator / control treatment
Placebo (Placebo suppository PR, 0.9% Normal Saline)
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Control group
Placebo
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Outcomes
Primary outcome [1]
397
0
Postoperative pain intensity
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Assessment method [1]
397
0
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Timepoint [1]
397
0
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Primary outcome [2]
398
0
Postoperative analgesic requirements
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Assessment method [2]
398
0
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Timepoint [2]
398
0
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Secondary outcome [1]
867
0
Side-effects of medications including nausea and vomiting
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Assessment method [1]
867
0
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Timepoint [1]
867
0
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Secondary outcome [2]
868
0
Sedation
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Assessment method [2]
868
0
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Timepoint [2]
868
0
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Eligibility
Key inclusion criteria
Consent to laparoscopic excision of suspected endometriosis. Capable to complete questions relating to pain, nausea and vomiting.
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Minimum age
18
Years
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Maximum age
45
Years
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Sex
Females
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Can healthy volunteers participate?
No
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Key exclusion criteria
Failure to give informed consent to participate in trialAllergy or hypersensitivity to amide type local anaestheticsContraindications to use of PR VoltarenPotential for drug interactions with the use of PR VoltarenKnown history of hypersensitivity to paracetamolContraindications to use of morphineSurgical procedure other than laparoscopic excision of endometriosisPregnancyActive or chronic relapsing pelvic inflammatory diseaseSuspected gynaecological malignancyCurrently on prescribed Codeine and/or prescribed OpiatesPlanned laparoscopic hysterectomyPoor comprehension of written and spoken English.
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Study design
Purpose of the study
Prevention
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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)
Central randomisation by phone
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
computer generated random number table
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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
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Type of endpoint/s
Efficacy
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Statistical methods / analysis
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Recruitment
Recruitment status
Recruiting
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Date of first participant enrolment
Anticipated
1/05/2004
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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
166
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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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Funding & Sponsors
Funding source category [1]
403
0
Commercial sector/Industry
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Name [1]
403
0
AGES Research Grant
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Address [1]
403
0
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Country [1]
403
0
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Primary sponsor type
Individual
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Name
Michael Costello
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Address
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Country
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Secondary sponsor category [1]
326
0
None
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Name [1]
326
0
Nil
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Address [1]
326
0
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Country [1]
326
0
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Ethics approval
Ethics application status
Approved
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Summary
Brief summary
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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
35660
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Address
35660
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Country
35660
0
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Phone
35660
0
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Fax
35660
0
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Email
35660
0
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Contact person for public queries
Name
9423
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Michael Costello
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Address
9423
0
Royal Hospital for Women
Barker St
Randwick NSW 2031
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Country
9423
0
Australia
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Phone
9423
0
02-93826677
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Fax
9423
0
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Email
9423
0
[email protected]
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Contact person for scientific queries
Name
351
0
Michael Costello
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Address
351
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Royal Hospital for Women
Barker St
Randwick NSW 2031
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Country
351
0
Australia
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Phone
351
0
02-93826677
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Fax
351
0
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Email
351
0
[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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