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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04813887
Other study ID # CHD21_0020
Secondary ID
Status Completed
Phase
First received
Last updated
Start date April 7, 2021
Est. completion date August 10, 2021

Study information

Verified date March 2021
Source Centre Hospitalier Departemental Vendee
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Pregnancy-induced physiological dermatological changes are common. In 2016, they represented between 23% (acne) and 75% (pigmentary changes) of pregnancies in France. Some dermatological changes require medical advice to identify a possible pathological rash. These pathological rashes can be dangerous for the mother or the fetus. The aim of this study is to assess the prevalence of skin diseases during pregnancy and to evaluate the care pathway in a healthcare sector (Vendee) for these pregnant women?


Description:

Pregnancy-induced physiological dermatological changes are common. In 2016, they represented between 23% (acne) and 75% (pigmentary changes) of pregnancies in France. Some dermatological changes require medical advice to identify a possible pathological rash. These pathological rashes can be dangerous for the mother or the fetus. It is therefore essential to recognize them for a quick specialized treatment. They include: intrahepatic cholestasis of pregnancy, pemphigoid gestationis, polymorphic eruption during pregnancy, atopic eczema, generalized pustular psoriasis in pregnancy. In view of the demography of dermatologists in the Vendee, 18 dermatologists in 2020 in all establishments (hospitals, clinics, practices), the general practitioner is at the center of these considerations. The aim of this study is to assess the situation of skin disease during pregnancy and to evaluate the care pathway in a healthcare sector (Vendee) for these pregnant women?


Recruitment information / eligibility

Status Completed
Enrollment 317
Est. completion date August 10, 2021
Est. primary completion date April 7, 2021
Accepts healthy volunteers No
Gender Female
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria: - Any woman who gives birth at Departmental Hospital Center of Vendee Exclusion Criteria: - Patient's refusal to participate in the study

Study Design


Related Conditions & MeSH terms


Intervention

Other:
questionnaire
Self-questionnaire on skin diseases reported during pregnancy

Locations

Country Name City State
France CHD Vendée La Roche sur Yon

Sponsors (1)

Lead Sponsor Collaborator
Centre Hospitalier Departemental Vendee

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Identify the health care provider that pregnant women consult when experiencing a skin disease Type of health care provider seeing a pregnant woman for skin disease after delivery during the patient's stay in the maternity (2-3 days)
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