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Trial registered on ANZCTR
Registration number
ACTRN12614000117617
Ethics application status
Approved
Date submitted
21/01/2014
Date registered
30/01/2014
Date last updated
30/01/2014
Type of registration
Retrospectively registered
Titles & IDs
Public title
Carbetocin versus syntometrine for prevention of postpartum hemorrhage after cesarean section
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Scientific title
Carbetocin versus syntometrine for prevention of postpartum hemorrhage after cesarean section
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Secondary ID [1]
283954
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none
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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:
postpartum hemorrhage
290977
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Condition category
Condition code
Reproductive Health and Childbirth
291320
291320
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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
single 100 microgram IV dose of carbetocin (Pabal) after fetal extraction and before placental removal
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Intervention code [1]
288642
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Prevention
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Intervention code [2]
288660
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Treatment: Drugs
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Comparator / control treatment
single dose IV combination of 5 IU oxytocin and 0.2 mg ergometrine after fetal extraction and before placental removal
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Control group
Active
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Outcomes
Primary outcome [1]
291312
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occurrence of postpartum hemorrhage (defined as a blood loss of greater than 1000 ml of blood following caesarean section)
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Assessment method [1]
291312
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Timepoint [1]
291312
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24 hours
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Secondary outcome [1]
306493
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need of additional oxytocic
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Assessment method [1]
306493
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Timepoint [1]
306493
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24 hours
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Secondary outcome [2]
306494
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side effects of drugs e.g. nausea, vomiting,metallic taste, shivering, flushing, headache, dizziness, dyspnea, and itching assessed by number of participants experienced that.
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Assessment method [2]
306494
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Timepoint [2]
306494
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24 hours
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Eligibility
Key inclusion criteria
37 – 40 weeks of gestational age
noncomplicated pregnancy.
Cesarean sections are a mixture of planned and emergency interventions under regional anaesthesia
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Minimum age
18
Years
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Maximum age
40
Years
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Sex
Females
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Can healthy volunteers participate?
Yes
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Key exclusion criteria
placenta previa
coagulopathy
preeclamptic
known sensitivity to oxytocin or methergine
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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)
numbered containers
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Simple randomisation using a randomisation table from a statistic book
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Masking / blinding
Blinded (masking used)
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Who is / are masked / blinded?
The people receiving the treatment/s
The people assessing the outcomes
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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
Completed
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Date of first participant enrolment
Anticipated
1/06/2011
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Actual
1/06/2011
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Date of last participant enrolment
Anticipated
30/05/2013
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Actual
30/05/2013
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Date of last data collection
Anticipated
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Actual
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Sample size
Target
450
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Accrual to date
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Final
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Recruitment outside Australia
Country [1]
5763
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Egypt
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State/province [1]
5763
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Cairo
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Funding & Sponsors
Funding source category [1]
288587
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Self funded/Unfunded
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Name [1]
288587
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Ahmed Maged
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Address [1]
288587
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135 king Faisal street, Haram Giza Egypt. postal code 12151
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Country [1]
288587
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Egypt
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Primary sponsor type
Individual
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Name
Ahmed Maged
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Address
Kasr Aini medical school . 135 king Faisal street, Haram Giza Egypt. postal code 12151
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Country
Egypt
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Secondary sponsor category [1]
287295
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Individual
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Name [1]
287295
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Ali abdelhafiz
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Address [1]
287295
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Kasr Aini medical school .1 Kasr Aini street Manial Cairo Egypt Postal code 12245
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Country [1]
287295
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Egypt
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
290450
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Kasr Aini local ethical committe
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Ethics committee address [1]
290450
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1 Kasr Aini street Manial Cairo Egypt Postal code 12245
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Ethics committee country [1]
290450
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Egypt
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Date submitted for ethics approval [1]
290450
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Approval date [1]
290450
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20/04/2011
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Ethics approval number [1]
290450
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Summary
Brief summary
A double blind randomized study conducted on 450 pregnant subjected randomly either to single 100 microgram IV dose of carbetocin (150 women) or combination of 5 IU oxytocin and 0.2 mg ergometrine (300 women) after fetal extraction and before placental removal to compare effectiveness and tolerability of carbetocin versus syntometrine in prevention of Postpartum hemorrhage after Cesarean section
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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
45758
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Prof Ahmed Maged
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Address
45758
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Kasr Aini medical school. 135 King faisal street , Haram , Giza Egypt. Postal code 12151
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Country
45758
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Egypt
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Phone
45758
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+2001005227404
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Fax
45758
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Email
45758
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[email protected]
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Contact person for public queries
Name
45759
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Ahmed Maged
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Address
45759
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Kasr Aini medical school.135 King faisal street , Haram , Giza Egypt. Postal code 12151
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Country
45759
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Egypt
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Phone
45759
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+2001005227404
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Fax
45759
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Email
45759
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[email protected]
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Contact person for scientific queries
Name
45760
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Ahmed Maged
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Address
45760
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Kasr Aini medical school. 135 King faisal street , Haram , Giza Egypt. Postal code 12151
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Country
45760
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Egypt
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Phone
45760
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+2001005227404
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Fax
45760
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Email
45760
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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
Source
Title
Year of Publication
DOI
Embase
Concerns about Data Integrity of 22 Randomized Controlled Trials in Women's Health.
2023
https://dx.doi.org/10.1055/s-0041-1727280
N.B. These documents automatically identified may not have been verified by the study sponsor.
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