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Trial registered on ANZCTR
Registration number
ACTRN12610001018000
Ethics application status
Approved
Date submitted
18/11/2010
Date registered
22/11/2010
Date last updated
22/11/2010
Type of registration
Prospectively registered
Titles & IDs
Public title
Misoprostol versus Oxytocin as prophylaxes against intraoperative and postoperative bleeding in cesarean section
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Scientific title
Misoprostol versus Oxytocin as prophylaxes against intraoperative and postoperative bleeding in cesarean section
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Secondary ID [1]
253120
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no secondary Id
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Universal Trial Number (UTN)
U1111-1118-2108
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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:
bleeding in cesarean section
258682
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Condition category
Condition code
Reproductive Health and Childbirth
258828
258828
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0
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Childbirth and postnatal care
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
600 microgram misoprostol (3 tablets) administrated rectally, right after induction of anesthesia.
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Intervention code [1]
257641
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Treatment: Drugs
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Intervention code [2]
257646
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Prevention
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Comparator / control treatment
10 ml oxytocin infused with 500 cc ringer solution right after clamping of the cord
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Control group
Active
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Outcomes
Primary outcome [1]
259690
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Intraoperative blood loss during Elective lower segment cesarean sections
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Assessment method [1]
259690
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Timepoint [1]
259690
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Number and weight differences of towels used intraoperatively
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Secondary outcome [1]
266387
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change in Hemoglobin levels pre and post operative
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Assessment method [1]
266387
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Timepoint [1]
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Measuring blood hemoglobin pre and post operative
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Eligibility
Key inclusion criteria
patients admitted for elective lower segment cesarean section
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Minimum age
15
Years
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Maximum age
45
Years
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Sex
Females
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Can healthy volunteers participate?
Yes
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Key exclusion criteria
patients with risk factors for postpartum hemorrhage, emergency lower segment cesarean section, or known hypersensitivity to prostaglandins.
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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)
Sealed opaque envelops (containers)
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Simple Randomization using a randomization table created by a computer software
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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
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
Not yet recruiting
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Date of first participant enrolment
Anticipated
1/12/2010
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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
220
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Accrual to date
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Final
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Recruitment outside Australia
Country [1]
3055
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Egypt
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State/province [1]
3055
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Cairo
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Funding & Sponsors
Funding source category [1]
258096
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Self funded/Unfunded
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Name [1]
258096
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Amany Sadek
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Address [1]
258096
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3/A, A.O.I buildings, Makram Ebad St., Nasr City, Cairo, Egypt
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Country [1]
258096
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Egypt
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Primary sponsor type
University
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Name
Ain Shams University
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Address
Ain Shams university Maternity Hospital, el demerdash Hospitals, El Abassia, Cairo, Egypt.
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Country
Egypt
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Secondary sponsor category [1]
257276
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None
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Name [1]
257276
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Address [1]
257276
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Country [1]
257276
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
260090
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Ain Shams Maternity Hospital Ethics committee
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Ethics committee address [1]
260090
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Ain Shams Maternity Hospital, Eldemerdash univeristy Hospital, El Abassia, Cairo, Egypt.
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Ethics committee country [1]
260090
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Egypt
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Date submitted for ethics approval [1]
260090
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Approval date [1]
260090
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13/10/2010
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Ethics approval number [1]
260090
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Summary
Brief summary
To compare the efficacy of rectally administrated Misoprostol vs. intravenous Oxytocin infusion during and after cesarean sections to control intraoperative and postoperative bleeding.
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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
31933
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Address
31933
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Country
31933
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Phone
31933
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Fax
31933
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Email
31933
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Contact person for public queries
Name
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Amany Sadek
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Address
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3/A, A.O.I. buildings, Makram Ebad St., Nasr city, Cairo, Egypt.
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Country
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Egypt
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Phone
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020 10 65 63 603
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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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Amany Sadek
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Address
6108
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3/A, A.O.I. buildings, Makram Ebad St., Nasr city, Cairo, Egypt.
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Country
6108
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Egypt
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Phone
6108
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020 10 65 63 603
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Fax
6108
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Email
6108
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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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