Oral Feeding During Established Labor at Our Institution
NCT ID: NCT03242356
Last Updated: 2018-04-13
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
195 participants
OBSERVATIONAL
2017-08-25
2017-11-25
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Interventions
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Questionnaire to assess of the application of the current French guidelines as to fasting during labor.
Questionnaire focuses on :
* oral intake of clear fluid during the labor
* oral intake of solid meal during the labor
* fasting duration for solid and liquids
* instruction received as to fasting during labor, nature of these instructions, and who given the instruction (midwife, nurse anesthetist, …)
* discomfort related to thirst during labor
* discomfort related to hunger during labor
We will also record several medical data as to the course of pregnancy and delivery, analgesia technique, history and characteristics of the parturient.
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
* Elective cesarean section, or emergency cesarean section in a woman not in labor
* Intrauterine fetal death
* Therapeutic abortion
* Patient consent not available (for example, in case of severe post-partum hemorrhage)
18 Years
FEMALE
No
Sponsors
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Hospices Civils de Lyon
OTHER
Responsible Party
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Locations
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hopital Femme Mère Enfant
Bron, , France
Countries
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Other Identifiers
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69HCL17_0454
Identifier Type: -
Identifier Source: org_study_id
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