Impact of General Practice Follow-up on Emergency Hospitalization of Patients Admitted for Chest Pain

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

RECRUITING

Total Enrollment

100 participants

Study Classification

OBSERVATIONAL

Study Start Date

2024-10-14

Study Completion Date

2025-07-31

Brief Summary

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This is a prospective observational study carried out in the emergency department of Emile Roux Hospital. Its aim is to compare the medical, psychological and social characteristics of patients followed up by a general practitioner and those without regular follow-up, using an anonymous questionnaire completed by the general practitioner in the emergency department, for patients consulting for the reason "chest pain".

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Detailed Description

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Conditions

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Chest Pain

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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Patient followed by a general practitionner

GP consulted in the last 12 months

Data collection

Intervention Type OTHER

Some data will be collected for all patients included: medical and family history, chest pain data and medical care data

Patient not followed by a general practitionner

Patient without regular follow-up

Data collection

Intervention Type OTHER

Some data will be collected for all patients included: medical and family history, chest pain data and medical care data

Interventions

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Data collection

Some data will be collected for all patients included: medical and family history, chest pain data and medical care data

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Patient admitted to Emile Roux hospital emergency department with chest pain
* Patient affiliated to the Social security system
* Patient able to give informed non-opposition to participating in research

Exclusion Criteria

* Patient under guardianship, curatorship, safeguard of justice or prisoners
* Patient with cognitive disorders
* Pregnant or breast-feeding women
* Refusal to participate

Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No