Management of Nausea and Vomiting in Pregnancy and Hyperemesis Gravidarum: Evaluation of Clinical Practices in Five Maternity Hospitals in Île-de-France

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

117 participants

Study Classification

OBSERVATIONAL

Study Start Date

2023-10-15

Study Completion Date

2024-03-15

Brief Summary

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This clinical trial aims to evaluate the adequacy of healthcare professionals' clinical practices regarding nausea and vomiting in pregnancy (NVP) and hyperemesis gravidarum (HG) with the recommendations of the National College of French Obstetricians and Gynecologists (CNGOF). The study involves 117 participants and follows an observational, cross-sectional, multicenter study design conducted in five maternity hospitals in Île-de-France.

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Detailed Description

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Conditions

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He Study Focuses on Evaluating Current Clinical Practices Rather Than Testing an Intervention

Study Design

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Observational Model Type

OTHER

Study Time Perspective

CROSS_SECTIONAL

Study Groups

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Midwives

Midwives involved in the care of patients suffering from nausea and vomiting of pregnancy and hypermesis gravidarum

No interventions assigned to this group

Obstetrician-Gynecologists

Obstetrician-Gynecologists involved in the care of patients suffering from nausea and vomiting of pregnancy and hypermesis gravidarum

No interventions assigned to this group

Gynecology-Obstetrics Interns

Gynecology-Obstetrics involved in the care of patients suffering from nausea and vomiting of pregnancy and hypermesis gravidarum

No interventions assigned to this group

Eligibility Criteria

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Inclusion Criteria

* Midwives, obstetrician-gynecologists, and gynecology-obstetrics interns working in the labor and delivery units, high-risk pregnancy units, and obstetric-gynecological emergency units of the five selected maternity hospitals.