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
NA
100 participants
INTERVENTIONAL
2024-05-01
2025-05-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
PREVENTION
DOUBLE
Study Groups
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Infrequent testing
Finger sticks every 4 hours in latent labor (less than 5cm cervical dilation) and every 2 hours in active labor (6cm and greater)
Fingerstick
Fingerstick to check glucose value during labor.
Frequent testing
Finger sticks every 2 hours in latent labor (less than 5cm cervical dilation) and every 1 hours in active labor (6cm and greater)
Fingerstick
Fingerstick to check glucose value during labor.
Interventions
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Fingerstick
Fingerstick to check glucose value during labor.
Eligibility Criteria
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Inclusion Criteria
* Patient with singleton gestation presenting in labor or for induction
Exclusion Criteria
* Multiple gestation pregnancy
* Patients undergoing scheduled c-section
18 Years
FEMALE
Yes
Sponsors
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Icahn School of Medicine at Mount Sinai
OTHER
Responsible Party
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Thomas Owens
Principal Investigator
Principal Investigators
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Thomas Owens, MD
Role: PRINCIPAL_INVESTIGATOR
Icahn School of Medicine at Mount Sinai
Locations
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Mount Sinai West Hospital
New York, New York, United States
Countries
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Other Identifiers
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STUDY-22-01607
Identifier Type: -
Identifier Source: org_study_id
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