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Trial registered on ANZCTR
Registration number
ACTRN12613001316796
Ethics application status
Approved
Date submitted
26/10/2013
Date registered
26/11/2013
Date last updated
26/11/2013
Type of registration
Prospectively registered
Titles & IDs
Public title
Endometrial preparation for cryo embryo transfer: effect of Gonadotropin Releasing Hormone Agonists (GnRHa) coupled with oestrogen and progesterone on hormonal profile and pregnancy rate
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Scientific title
The effect of endometrial preparation by pretreatment with Gonadotrophin-releasing hormone agonist (GnRha), oestrogen and progesterone, compared to endometrial preparation by oestrogen and progesterone only, on clinical pregnancy rate in infertile couples undergoing cryo embryo transfer as treatment for infertility
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Secondary ID [1]
283460
0
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:
Infertility
290379
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Condition category
Condition code
Reproductive Health and Childbirth
290769
290769
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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
Group B (intervention group):
Patient will be treated with the GnRh-analouge, triptorelin 0.1mg/day subcutaneously beginning in the mid luteal phase of the previous menstrual cycle and continuing till the date of embryo transfer. Full pituitary desensitization will be ensured by measuring serum estradiol on the first day of the menstrual cycle and should be less than 50 picogram /dl
Endometrial preparation will begin from third day of menstruation by oral Estradiol valerate 8mg/day till endomtrium exceeding 8.5mm, then progesterone administration rectal suppository 400mg Am and intramuscular 100mg Pm.
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Intervention code [1]
288173
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Treatment: Drugs
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Comparator / control treatment
Group A (control group): Endometrial preparation will begin from third day of menstruation by oral Estradiol valerate 8mg/day till endomtrium exceeding 8.5mm, then progesterone administration rectal suppository 400mg Am and intramuscular 100mg Pm .
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Control group
Active
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Outcomes
Primary outcome [1]
290765
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clinical pregnancy rate by
1. serum human chorionic gonadotropin (hCG) assay 14 days after embryo transfer
2. Vaginal ultrasound 2 weeks after a positive pregnancy test to detect cardiac pulsation
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Assessment method [1]
290765
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Timepoint [1]
290765
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The primary time point (clinical pregnancy rate) is assessed 2 weeks after the frozen embryo transfer. The whole study will take a one year duration
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Secondary outcome [1]
305236
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none
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Assessment method [1]
305236
0
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Timepoint [1]
305236
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none
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Eligibility
Key inclusion criteria
1. Age: 35 years old or less.
2. Infertility: primary or secondary
3. Embryos: were frozen on day five.
4. Cryopreservation: closed method vitrification
5. Laser assisted hatching prior to embryo transfer.
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Minimum age
18
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
1. Age above 35 years old.
2. Abnormal uterine factor diagnosed by Vaginal sonography, Hysteroscopy or Hysterosalpingography
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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
Blinded (masking used)
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Who is / are masked / blinded?
The people analysing the results/data
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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
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
1/12/2013
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Actual
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Date of last participant enrolment
Anticipated
1/01/2015
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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
140
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Accrual to date
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Final
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Recruitment outside Australia
Country [1]
5538
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Egypt
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State/province [1]
5538
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Alexandria
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Funding & Sponsors
Funding source category [1]
288171
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Hospital
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Name [1]
288171
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Elshatby University Maternity Hospital
Department of Obstetrics and Gynecology
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Address [1]
288171
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Elshatby University Maternity Hospital
Department of Obstetrics and Gynecology
Elshatby
PO Box; 23615
Alexandria
Egypt
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Country [1]
288171
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Egypt
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Primary sponsor type
Hospital
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Name
Elshatby University Maternity Hospital Department of Obstetrics and Gynecology
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Address
Elshatby University Maternity Hospital
Department of Obstetrics and Gynecology
Elshatby
PO Box; 23615
Alexandria
Egypt
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Country
Egypt
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Secondary sponsor category [1]
286894
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None
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Name [1]
286894
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Address [1]
286894
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Country [1]
286894
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Ethics approval
Ethics application status
Approved
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Summary
Brief summary
The aim of the work is compare artificial endometrial preparation by oestrogen and progesterone versus pretreatment with Gonadotrophin-releasing hormone agonist (GnRha), oestrogen and progesterone for cryo embryo transfer according to clinical pregnancy rate.
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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
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A/Prof Yasser Ibrahim Orief
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Address
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Dr Yasser orief
El-Mosheer Ahmed Ismaiel St.,
Panorama Elshark Building
Sidi Gaber Elshiekh tram station above HSBC bank
PO box: 21615
Alexandria
Egypt.
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Country
43866
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Egypt
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Phone
43866
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+20 100 8233 121
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Fax
43866
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+20 3 544 22 64 (extension 102)
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Email
43866
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[email protected]
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Contact person for public queries
Name
43867
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Yasser Ibrahim Orief
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Address
43867
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Dr Yasser orief
El-Mosheer Ahmed Ismaiel St.,
Panorama Elshark Building
Sidi Gaber Elshiekh tram station above HSBC bank
PO box: 21615
Alexandria
Egypt.
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Country
43867
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Egypt
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Phone
43867
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+20 100 8233 121
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Fax
43867
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+20 3 544 22 64 (extension 102)
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Email
43867
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[email protected]
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Contact person for scientific queries
Name
43868
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Yasser Ibrahim Orief
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Address
43868
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Dr Yasser orief
El-Mosheer Ahmed Ismaiel St.,
Panorama Elshark Building
Sidi Gaber Elshiekh tram station above HSBC bank
PO box: 21615
Alexandria
Egypt.
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Country
43868
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Egypt
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Phone
43868
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+20 100 8233 121
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Fax
43868
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+20 3 544 22 64 (extension 102)
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Email
43868
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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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