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Recruiting NCT06693063

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

Observational Chest Pain

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Data collection.
Who it may be relevant to
Registry conditions: Chest Pain. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
France
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

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".

Interventions

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

Primary outcome measures

  • Compare the hospitalization rate of patients admitted for chest pain, according to their medical follow-up by a general practitioner. [Time frame: Only once, within 24 hours of admission to the emergency department]
Secondary outcome measures (1)
  • Describe the population of patients admitted to the Emile Roux hospital emergency department with chest pain and followed by a general practitioner versus those without medical follow-up. [Time frame: Only once, within 24 hours of admission to the emergency department]

Eligibility criteria

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

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Cohort

Study locations

France · 1 center
  • Centre Hospitalier Emile Roux — Le Puy-en-Velay

Identifiers

NCT: NCT06693063 · EDS_2024_douleurthoracique

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗