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
100 participants
INTERVENTIONAL
2020-03-01
2022-03-01
Brief Summary
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Detailed Description
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Conditions
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Study Design
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NA
SINGLE_GROUP
OTHER
NONE
Study Groups
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performing US scans for fetal weight assessment.
SAMPL plain wave algorithm
SAMPL's plain-wave algorithm allowing portable US or Wireless Probe scanning - thus enabling clinicians with more flexible point-of-care locations when performing US scans for fetal weight assessment.
Interventions
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SAMPL plain wave algorithm
SAMPL's plain-wave algorithm allowing portable US or Wireless Probe scanning - thus enabling clinicians with more flexible point-of-care locations when performing US scans for fetal weight assessment.
Eligibility Criteria
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Inclusion Criteria
2. Women with a singleton viable pregnancy.
Exclusion Criteria
18 Years
45 Years
FEMALE
Yes
Sponsors
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Hillel Yaffe Medical Center
OTHER_GOV
Responsible Party
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Principal Investigators
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Alon Shrim, MD
Role: PRINCIPAL_INVESTIGATOR
Hillel Yaffe Medical Center
Locations
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Hille Yaffe Medical Center
Hadera, , Israel
Countries
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Central Contacts
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Other Identifiers
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0108-18-HYMC
Identifier Type: -
Identifier Source: org_study_id
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