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Trial registered on ANZCTR
Registration number
ACTRN12611000639921
Ethics application status
Approved
Date submitted
22/06/2011
Date registered
23/06/2011
Date last updated
23/06/2011
Type of registration
Retrospectively registered
Titles & IDs
Public title
Comparison between two clomiphene citrate protocols for induction of ovulation in clomiphene resistant Polycystic ovarian disease.
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Scientific title
Comparison between two clomiphene citrate protocols for induction of ovulation in clomiphene resistant Polycystic ovarian disease.
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Secondary ID [1]
262430
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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:
Polycystic ovarian disease.
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Resistant Anovulation
268136
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Condition category
Condition code
Reproductive Health and Childbirth
268267
268267
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0
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Fertility including in vitro fertilisation
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
clomiphene citrate oral tablets 100 mg daily for 10 days, starting within 5 days of induced menses.
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Intervention code [1]
266802
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Treatment: Drugs
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Comparator / control treatment
control group clomiphene citrate oral tablets 200 mg daily for 5 days, starting within 5 days of induced menses.
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Control group
Dose comparison
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Outcomes
Primary outcome [1]
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ovulation detected by transvaginal follicle scanning, and serum progesterone value.
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Assessment method [1]
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Timepoint [1]
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after the end of treatment
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Secondary outcome [1]
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chemical pregnancy by serum HCG assay.
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Assessment method [1]
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Timepoint [1]
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after the end of cycle
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Secondary outcome [2]
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clinical pregnancy by ultrasonography.
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Assessment method [2]
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Timepoint [2]
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2 weeks after serum pregnancy test.
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Eligibility
Key inclusion criteria
married, nulligravida, polycystic ovarian disease, resistant to clomiphene citrate drug in previous cycle/s
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Minimum age
20
Years
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Maximum age
35
Years
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Sex
Females
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Can healthy volunteers participate?
No
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Key exclusion criteria
previous pelvic surgery, other causes of infertility, BMI>35
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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)
Evaluation of eligibility, informed consent.
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Randomization using computer generated tables, results kept in sealed envelopes till the time of starting treatment.
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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
Completed
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Date of first participant enrolment
Anticipated
1/01/2009
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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
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Actual
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Sample size
Target
200
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Accrual to date
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Final
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Recruitment outside Australia
Country [1]
3637
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Egypt
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State/province [1]
3637
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Funding & Sponsors
Funding source category [1]
267278
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Self funded/Unfunded
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Name [1]
267278
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Address [1]
267278
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Country [1]
267278
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Egypt
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Primary sponsor type
Individual
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Name
Mervat Sheikh Elarab Elsedeek Omran
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Address
649 Elhorreya street, Janaclis, Elraml District, Alexandria Egypt.
post code 03312
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Country
Egypt
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Secondary sponsor category [1]
266338
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None
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Name [1]
266338
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Address [1]
266338
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Country [1]
266338
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
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The ethics committee of Alexandria faculty of medicine, Alexandria university.
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Ethics committee address [1]
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Alexandria faculty of Medicine, Elraml district, Alexandria, Egypt. post code 03312
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Ethics committee country [1]
269272
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Egypt
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Date submitted for ethics approval [1]
269272
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Approval date [1]
269272
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29/05/2008
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Ethics approval number [1]
269272
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Summary
Brief summary
The primary purpose of the study is to test if either doubling the dose of clomiphene citrate or doubling the duration would make previously unresponsive patients respond and ovulate, and to compare the efficacy of either approach.
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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
32764
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Address
32764
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Country
32764
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Phone
32764
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Fax
32764
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Email
32764
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Contact person for public queries
Name
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Mervat Sheikh elarab Elsedeek
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Address
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649 Elhorreya street, Janaclis, Elraml District, Alexandria Egypt.
post code 03312
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Country
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Egypt
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Phone
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+203 5759915
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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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Mervat Sheikh elarab Elsedeek
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Address
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649 Elhorreya street, Janaclis, Elraml District, Alexandria Egypt.
post code 03312
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Country
6939
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Egypt
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Phone
6939
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+203 5759915
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Fax
6939
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Email
6939
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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
Dimensions AI
Comparison between two clomiphene citrate protocols for induction of ovulation in clomiphene resistant polycystic ovary syndrome
2014
https://doi.org/10.1016/j.mefs.2013.05.012
N.B. These documents automatically identified may not have been verified by the study sponsor.
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