Endometrial Biopsy Protocol for In Vitro Fertilization (IVF)
NCT ID: NCT01278706
Last Updated: 2011-01-26
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
NA
200 participants
INTERVENTIONAL
2011-01-31
Brief Summary
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In this study, the investigators will compare different temporal timing of the biopsies with regards to the menstrual cycle and their affect on the success rates of the treatment.
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
NONE
Study Groups
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no treatment
No interventions assigned to this group
one biopsy, proliferative phase
endometrial biopsy/ies
performing office endometrial biopsy with a disposable sterile catheter
one biopsy, secretory phase
endometrial biopsy/ies
performing office endometrial biopsy with a disposable sterile catheter
two biopsies
endometrial biopsy/ies
performing office endometrial biopsy with a disposable sterile catheter
Interventions
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endometrial biopsy/ies
performing office endometrial biopsy with a disposable sterile catheter
Eligibility Criteria
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Inclusion Criteria
* between 1-6 previous failed IVF cycles
* normal hormonal profile
Exclusion Criteria
* hydrosalpinx
* intrauterine lesion /malformation
18 Years
38 Years
FEMALE
Yes
Sponsors
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Kaplan Medical Center
OTHER
Responsible Party
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Kaplan Medical Center
Locations
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Kaplan Medical Center, IVF Unit
Rehovot, , Israel
Weizmann Institute of Science
Rehovot, , Israel
Countries
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Central Contacts
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Facility Contacts
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Levin
Role: primary
Other Identifiers
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kmc110154CTIL
Identifier Type: -
Identifier Source: org_study_id
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