Evaluation of the Rate of Consultations in Gynecological Emergencies Under "Non-urgent" Management

Gynecologic Disease Clinical Trial

— URGO_CARE  

Official title:

City-hospital Network: Evaluation of the Rate of Consultations in Gynecological Emergencies Under Non-emergency Management

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT05325619
• Other study ID #: URGO_CARE
• Status: Completed
• Start date: March 23, 2022
• Est. completion date: August 2, 2022

Study information

• Verified date: March 2023
• Source: Groupe Hospitalier Paris Saint Joseph
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

The difference between the demand and the current medical supply poses a real public health problem in terms of the organization of health care systems.

For several years in France, there has been an increase in the number of consultations in emergency services, particularly gynaecological ones. The two causes put forward are a change in user behavior with an increase in requests for rapid but "non-urgent" care and the inadequacy of the supply of care in the private sector.

Few studies have been carried out concerning gynaecological emergencies, unlike general emergencies.

The aim of this study is to measure the frequency of consultations in gynaecological emergencies for non-emergency reasons.

The interest of this study is therefore mainly on the optimization of the care system with the emphasis on the city-hospital network in the management of these patients.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 809
• Est. completion date: August 2, 2022
• Est. primary completion date: July 24, 2022
• Accepts healthy volunteers: No
• Gender: Female
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Patient whose age is = 18 years

• Patient not pregnant or pregnant < 14 SA

• Patient admitted for gynecological emergency care at Paris Saint-Joseph Hospital between 01/02/2021 and 30/04/2021

• French-speaking patient

Exclusion Criteria:

• Patient under guardianship or curatorship

• Patient deprived of liberty

• Patient under court protection

• Patient objecting to the use of her data for this research

Related Conditions & MeSH terms

• Emergencies
• Gynecologic Disease

Locations

Country	Name	City	State
France	Groupe Hospitalier Paris Saint-Joseph	Paris

Sponsors (1)

Lead Sponsor	Collaborator
Groupe Hospitalier Paris Saint Joseph

Country where clinical trial is conducted

France, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Rate of gynecological emergency room visits for non-urgent reasons	This outcome corresponds to number of non-emergency gynecological emergency visits out of the total number of gynecological emergencies.	Month 2
Secondary	Optimization of patient care not requiring urgent care	This outcome corresponds to the the number of patients who were referred to semi-emergency or semi-programmed care facilities.	Month 2
Secondary	Hospitalization rate	This outcome corresponds to the number of women hospitalized.	Month 2
Secondary	Surgical management rate	This outcome corresponds to the number of women who are operated.	Month 2

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