Chest PainNCT06693063
Impact of General Practice Follow-up on Emergency Hospitalization of Patients Admitted for Chest Pain
An observational study of Chest Pain, run by Centre Hospitalier Emile Roux at 1 site in France.
Trial summary
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… Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Chest Pain
- What is being tested?
- Data collection
- How many people
- 100 participants
- Where
- 1 siteFrance
- Study dates
- 14 Oct 2024to Jul 2025
- Phase
- Observational
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Study population: Patient admitted to Emile Roux hospital emergency department with chest pain
Who may be able to join
- 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
Who cannot join
- Patient under guardianship, curatorship, safeguard of justice or prisoners
- Patient with cognitive disorders
- Pregnant or breast-feeding women
- Refusal to participate
Trial locations and contacts
1 site in 1 country. Contact the study team or a site near you to ask about taking part.
Marlène BONNEFOI contact
France1 site, 1 recruiting
- Recruiting
Centre Hospitalier Emile Roux
Le Puy-en-Velay, 43000
Luc PIGEON, MD, +33471043885, luc.pigeon@ch-lepuy.fr
Arnaud JOLLET, arnaud.jollet@ch-lepuy.fr
About this study
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".
- Conditions
- Chest Pain
- Being tested
- Data collection
- Keywords
- emergency admission, general practitioner
- Medical subject headings
- Chest Pain
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Data collectionOther
Some data will be collected for all patients included: medical and family history, chest pain data and medical care data
| Study group | Role | What they receive |
|---|---|---|
| Patient followed by a general practitionner | GP consulted in the last 12 months Receives: Other: Data collection | |
| Patient not followed by a general practitionner | Patient without regular follow-up Receives: Other: Data collection |
What is being measured
The primary outcome is the main question the study is designed to answer.
Compare the hospitalization rate of patients admitted for chest pain, according to their medical follow-up by a general practitioner.
Measured: Only once, within 24 hours of admission to the emergency department
Secondary outcomes (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.
Measured: Only once, within 24 hours of admission to the emergency department
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted18 Nov 2024
- Study start14 Oct 2024
- Primary completionJul 2025 (estimated)
- Study completionJul 2025 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Chest PainStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Cohort
- Time perspective
- Prospective
- Enrolment
- 100 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Centre Hospitalier Emile Roux
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
- Investigators
- Luc PIGEON, Principal investigator, Hospital Center Emile Roux, Le Puy-en-Velay (France)
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06693063
- Sponsor's protocol ID
- EDS_2024_douleurthoracique
- Status last verified
- Nov 2024
- First submitted
- 8 Nov 2024
- Last updated
- 18 Nov 2024
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Undecided
Study at a glance
From the registry record, last updated by the sponsor on 18 Nov 2024. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Impact of General Practice Follow-up on Emergency Hospitalization of Patients Admitted for Chest Pain
- ClinicalTrials.gov ID
- NCT06693063
- Acronym / sponsor ID
- EDS_2024_douleurthoracique
- Conditions
- Chest Pain
- Keywords
- emergency admission, general practitioner
- Study type
- Observational
- Recruitment status
- Recruiting
- Enrolment
- 100 participants (estimated)
- Lead sponsor
- Centre Hospitalier Emile RouxUniversity, hospital or other
- Study start
- 14 Oct 2024 (actual)
- Primary completion
- Jul 2025 (estimated)
- Study completion
- Jul 2025 (estimated)
- First posted
- 18 Nov 2024 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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 design
- Observational model
- Cohort
- Time perspective
- Prospective
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Patient followed by a general practitionner | – | Other: Data collectionGP consulted in the last 12 months |
| Patient not followed by a general practitionner | – | Other: Data collectionPatient without regular follow-up |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
- Study population
- Patient admitted to Emile Roux hospital emergency department with chest pain
Key inclusion criteria (3 listed)
- 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
Key exclusion criteria (4 listed)
- Patient under guardianship, curatorship, safeguard of justice or prisoners
- Patient with cognitive disorders
- Pregnant or breast-feeding women
- Refusal to participate
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Data collectionSome data will be collected for all patients included: medical and family history, chest pain data and medical care data | Other | Patient followed by a general practitionner, Patient not followed by a general practitionner |
Primary outcome
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
1 secondary outcome
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
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 18 Nov 2024.
- Individual participant dataSharing planned: Undecided
Related trials for Chest Pain
Not yet recruiting
Effect of Warm Footbath Combined With Relaxation Exercise on Pain and Anxiety During Chest Tube Removal After Cardiac Surgery
Chest Tube Removal
Not yet recruiting
Lung Cancer and Aging: Improving Well-being for Older Adults With Lung Cancer
Lung Cancer
Recruiting
CT Stress Myocardial Perfusion, Fractional Flow Reserve and Angiography in Patients With Stable Chest Pain Syndromes
Coronary Artery Disease, Chest Syndrome
RecruitingPhase 4
Early Single Antiplatelet Therapy After IVUS-Guided PCI in Acute Coronary Syndrome
Acute Coronary Syndromes, STEMI
Recruiting
AI-Assisted Interpretation of Cardiac CT in the Emergency Department
Chest Pain, Acute Coronary Syndrome
Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
Marlène BONNEFOI contact
Luc PIGEON principal investigator
Hospital Center Emile Roux, Le Puy-en-Velay (France)
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Chest Pain, run by Centre Hospitalier Emile Roux at 1 site in France.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 3 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: looking for participants now, as of the sponsor's last update on 18 Nov 2024. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in France. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Contact Luc PIGEON, MD (+33471043885, luc.pigeon@ch-lepuy.fr), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
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). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 18 Nov 2024.