Oral Feeding During Established Labor at Our Institution

NCT ID: NCT03242356

Last Updated: 2018-04-13

Study Results

Results pending

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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Recruitment Status

COMPLETED

Total Enrollment

195 participants

Study Classification

OBSERVATIONAL

Study Start Date

2017-08-25

Study Completion Date

2017-11-25

Brief Summary

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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).

Detailed Description

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Conditions

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Labor

Study Design

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Observational Model Type

COHORT

Study Time Perspective

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.

Intervention Type OTHER

Eligibility Criteria

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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)
Minimum Eligible Age

18 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

No

Sponsors

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Hospices Civils de Lyon

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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hopital Femme Mère Enfant

Bron, , France

Site Status

Countries

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France

Other Identifiers

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69HCL17_0454

Identifier Type: -

Identifier Source: org_study_id

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