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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COMPLETED
200 participants
OBSERVATIONAL
2020-12-31
2021-03-11
Brief Summary
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Detailed Description
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Informed consent is not required due to the retrospective nature of the study. Patient information including medical, obstetric and general background will be collected.
Conditions
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Study Design
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COHORT
RETROSPECTIVE
Study Groups
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Women of short stature
Women that are under 1.6 meters.
Analysis of a patient registry
Analysis of a patient registry.
Interventions
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Analysis of a patient registry
Analysis of a patient registry.
Eligibility Criteria
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Inclusion Criteria
* Singleton pregnancy.
* Low risk pregnancy.
* Accurate dating.
Exclusion Criteria
* Multiple pregnancy.
* High risk pregnancy.
18 Years
45 Years
FEMALE
No
Sponsors
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Rambam Health Care Campus
OTHER
Responsible Party
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ROY LAUTERBACH MD
Principal Investigator
Principal Investigators
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Roy Lauterbach, MD
Role: PRINCIPAL_INVESTIGATOR
Rambam healthcare campus
Locations
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Rambam health care campus
Haifa, , Israel
Countries
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Other Identifiers
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0275-19-RMB
Identifier Type: -
Identifier Source: org_study_id
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