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Oral Feeding During Established Labor at Our Institution

Oral Feeding During Established Labor. Current Practices in the Obstetric Department of the Femme Mère Enfant Hospital (Lyon, France)

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03242356
Enrollment
195
Registered
2017-08-08
Start date
2017-08-25
Completion date
2017-11-25
Last updated
2018-04-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Labor

Brief summary

Current French guidelines allow oral intake of clear fluid in women in established labor under epidural analgesia. To date, no study assessed how these guidelines are followed in clinical practice. This study aims to assess the current practices as to the fasting during the labor at our institution, while assessing the experience and the expectations of the parturients (level of comfort or discomfort related to fasting).

Interventions

OTHERQuestionnaire 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.

Sponsors

Hospices Civils de Lyon
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* All adult woman who has been in labor in our hospital

Exclusion criteria

* Patient refusal * 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)

Design outcomes

Primary

MeasureTime frame
Rate of parturients who declared to have ingested clear fluid during the labor.The survey will be completed within 2 hours following the delivery

Secondary

MeasureTime frameDescription
Specify the type of liquid ingested (water or sweet liquid) and its volumeThe survey will be completed within 2 hours following the deliveryNature and volume of liquids ingested
Specify the frequency of ingestion of solid foods during laborThe survey will be completed within 2 hours following the deliveryNature and quantity of ingested solids
Assess the degree of discomfort associated with thirst that was felt during laborThe survey will be completed within 2 hours following the deliveryDegree of discomfort related to thirst on a simple numeric scale (0: no discomfort at 10: very uncomfortable)
Assess the degree of discomfort associated with hunger that was felt during laborThe survey will be completed within 2 hours following the deliveryDegree of discomfort related to hunger on a simple numeric scale (0: no discomfort at 10: very uncomfortable)
Determine the instructions given by health professionals, their spontaneous or non-spontaneous character and the information related to the given fast, according to the parturientThe survey will be completed within 2 hours following the deliveryDetermine the instructions given by health professionals, whether they are spontaneous or not
Determine if nausea and vomiting are more common in women who have ingested fluids during laborThe survey will be completed within 2 hours following the deliveryIncidence of at least one episode of nausea and vomiting during labor
Analyze the factors associated with fasting during work and their concordance with the French recommendations on fasting during laborThe survey will be completed within 2 hours following the deliveryAnalysis of independent risk factors for the patient's strict fasting during labor
Indicate the total duration of fast and solid fasting before birthThe survey will be completed within 2 hours following the deliveryTotal duration of liquid fasting and solids preceding birth
Compare fasting instructions received by patients and practices reported by professionalsThe survey will be completed within 2 hours following the deliveryFasting instructions received by patients and practices reported by professionals obtained during a practice survey
Evaluate women's satisfaction with the fasting instructions receivedThe survey will be completed within 2 hours following the deliverySatisfaction with fasting instructions given on a simple numerical scale (0: very high dissatisfaction, 10: maximum satisfaction)

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026