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

C

Centre Hospitalier de Saint-Denis

Status

Completed

Conditions

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

Study type

Observational

Funder types

Other

Identifiers

NCT06841029
0051_MATERNITE_

Details and patient eligibility

About

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.

Enrollment

117 patients

Sex

All

Volunteers

No Healthy Volunteers

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.

Exclusion criteria

  • Midwives or doctors in training (student midwives or medical externs)
  • Midwives and obstetrician-gynecologists working in private practice

Trial design

117 participants in 3 patient groups

Midwives
Description:
Midwives involved in the care of patients suffering from nausea and vomiting of pregnancy and hypermesis gravidarum
Obstetrician-Gynecologists
Description:
Obstetrician-Gynecologists involved in the care of patients suffering from nausea and vomiting of pregnancy and hypermesis gravidarum
Gynecology-Obstetrics Interns
Description:
Gynecology-Obstetrics involved in the care of patients suffering from nausea and vomiting of pregnancy and hypermesis gravidarum

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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