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

Sponsor
Groupe Hospitalier Paris Saint Joseph (Other)
Overall Status
Recruiting
CT.gov ID
NCT05325619
Collaborator
(none)
1,300
1
9.3
139.8

Study Details

Study Description

Brief 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.

Condition or Disease Intervention/Treatment Phase

    Study Design

    Study Type:
    Observational
    Anticipated Enrollment :
    1300 participants
    Observational Model:
    Cohort
    Time Perspective:
    Retrospective
    Official Title:
    City-hospital Network: Evaluation of the Rate of Consultations in Gynecological Emergencies Under Non-emergency Management
    Actual Study Start Date :
    Mar 23, 2022
    Anticipated Primary Completion Date :
    Jul 24, 2022
    Anticipated Study Completion Date :
    Dec 31, 2022

    Outcome Measures

    Primary Outcome Measures

    1. Rate of gynecological emergency room visits for non-urgent reasons [Month 2]

      This outcome corresponds to number of non-emergency gynecological emergency visits out of the total number of gynecological emergencies.

    Secondary Outcome Measures

    1. Optimization of patient care not requiring urgent care [Month 2]

      This outcome corresponds to the the number of patients who were referred to semi-emergency or semi-programmed care facilities.

    2. Hospitalization rate [Month 2]

      This outcome corresponds to the number of women hospitalized.

    3. Surgical management rate [Month 2]

      This outcome corresponds to the number of women who are operated.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    Female
    Accepts Healthy Volunteers:
    No
    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

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Groupe Hospitalier Paris Saint-Joseph Paris France 75014

    Sponsors and Collaborators

    • Groupe Hospitalier Paris Saint Joseph

    Investigators

    • Principal Investigator: Marie Charlotte Marie Charlotte, MD, Groupe Hospitalier Paris Saint Joseph

    Study Documents (Full-Text)

    None provided.

    More Information

    Additional Information:

    Publications

    None provided.
    Responsible Party:
    Groupe Hospitalier Paris Saint Joseph
    ClinicalTrials.gov Identifier:
    NCT05325619
    Other Study ID Numbers:
    • URGO_CARE
    First Posted:
    Apr 13, 2022
    Last Update Posted:
    Jun 30, 2022
    Last Verified:
    Jun 1, 2022
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Jun 30, 2022