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

November 15, 2024 updated by: Centre Hospitalier Emile Roux
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".

Study Overview

Status

Recruiting

Conditions

Intervention / Treatment

Study Type

Observational

Enrollment (Estimated)

100

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Contact Backup

Study Locations

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Sampling Method

Non-Probability Sample

Study Population

Patient admitted to Emile Roux hospital emergency department with chest pain

Description

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

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Patient followed by a general practitionner
GP consulted in the last 12 months
Other: Data collection
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
Other: Data collection
Some data will be collected for all patients included: medical and family history, chest pain data and medical care data

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
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
Only once, within 24 hours of admission to the emergency department

Secondary Outcome Measures

Outcome Measure
Time Frame
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
Only once, within 24 hours of admission to the emergency department

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Centre Hospitalier Emile Roux

Investigators

  • Principal Investigator: Luc PIGEON, Hospital Center Emile Roux, Le Puy-en-Velay (France)

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

October 14, 2024

Primary Completion (Estimated)

July 1, 2025

Study Completion (Estimated)

July 1, 2025

Study Registration Dates

First Submitted

November 8, 2024

First Submitted That Met QC Criteria

November 15, 2024

First Posted (Estimated)

November 18, 2024

Study Record Updates

Last Update Posted (Estimated)

November 18, 2024

Last Update Submitted That Met QC Criteria

November 15, 2024

Last Verified

November 1, 2024

More Information

Terms related to this study

Keywords

Additional Relevant MeSH Terms

Other Study ID Numbers

  • EDS_2024_douleurthoracique

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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