NCT06859021

Brief Summary

The lifetime prevalence of chest pain in the general population is 20-40%. The etiologies to be evoked from the outset of management are those of cardiovascular origin, such as acute coronary syndrome (ACS) and pulmonary embolism. ACS is responsible for almost 20% of deaths. Delay in treatment is a major prognostic factor, given the importance of coronary reperfusion. In France, one of the first contacts with the healthcare system is the medical regulation assistant (MRA) at the Centre 15. His or her role is to prioritize the call according to the identification of immediate signs of seriousness, and if necessary, to decide autonomously to send a rescue team before medical regulation. Depending on the reason for the call and any signs of seriousness, it prioritizes the call according to the expected response time. In line with current recommendations, all calls for chest pain should be answered by an emergency medical dispatcher (EMR) within 5 minutes. However, 60-90% of chest pain calls are not of cardiovascular origin. Their prioritization could therefore be re-qualified for longer response times. Given the frequency of this type of call, a more efficient MRA referral strategy is needed. To achieve this, decision-support tools would be essential. The performance of the HAR (History, Age and Risk Factors) score has been recently explored, derived from the HEART score, in a previous single-center prospective study in 2019. It stratifies the risk of a major cardiovascular event (MCE) into low (0 or 1 point), intermediate (2 or 3 points) or high (4, 5 or 6 points). Investigator's hypothesis is that the HAR score could be entrusted to MRA, to enable them to optimize the prioritization of patients calling with non-traumatic chest pain, by qualifying low-risk chest pain calls on the one hand, which could be prioritized in P2 SNP, and high-risk calls on the other, making it possible to anticipate the dispatch of an emergency service.

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
796

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started May 2025

Shorter than P25 for all trials

Geographic Reach
1 country

3 active sites

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

February 28, 2025

Completed
5 days until next milestone

First Posted

Study publicly available on registry

March 5, 2025

Completed
2 months until next milestone

Study Start

First participant enrolled

May 2, 2025

Completed
7 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 1, 2025

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2025

Completed
Last Updated

March 24, 2025

Status Verified

March 1, 2025

Enrollment Period

7 months

First QC Date

February 28, 2025

Last Update Submit

March 19, 2025

Conditions

Keywords

ChestpainHAR scoreEmergency call

Outcome Measures

Primary Outcomes (1)

  • Number of major cardiovascular events

    Number of major cardiovascular events is measured by presence of Death from cardiological causes, Type 1 or 2 myocardial infarction, Percutaneous coronary intervention, Surgical coronary bypass surgery

    30 days

Secondary Outcomes (4)

  • Performance of the HAR Score: Sensitivity, Specificity, and Comparison Between EMR and MRA

    From Day 0 to Day 30

  • Comparaison between rescue resources decided and predicted by the HAR score

    From Day 0 to Day 30

  • Time delta between the end of the MRA's score suggesting the dispatch of equipment (HAR score ≥ 4 points) and the actual decision to dispatch equipment in the current situation.

    From Day 0 to Day 30

  • Area under the ROC curve and Delong-Delong test

    From Day 0 to Day 30

Study Arms (1)

call for chest pain

patients who call for chest pain

Other: follow up call

Interventions

A follow-up call is made to the patient 30 days (+ 5 days) after inclusion to check for the occurrence of an Major Cardio Vascular Event.

call for chest pain

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Patients calling center 15 for chest pain

You may qualify if:

  • Patient of legal age (≥ 18 years)
  • Calling Center 15 from 49, 72 or 37
  • Expressing non-traumatic chest pain, even if this is not the main reason for seeking help.

You may not qualify if:

  • Treatment in departments other than 49, 72 and 37
  • Taken in charge in an emergency department of a private facility in the 49, 72 and 37 départements
  • Poor understanding of the French language
  • Non-affiliated or non-beneficiary of a social security scheme
  • Person deprived of liberty by judicial or administrative decision
  • Person under forced psychiatric care
  • Person subject to a legal protection measure
  • Person unable to express his/her non-opposition.
  • Follow-up at Day 30 impossible for any reason
  • Person having expressed his/her opposition to the collection of his/her data.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (3)

Centre Hospitalier Universitaire d'Angers

Angers, 49000, France

Location

Centre Hospitalier Le Mans

Le Mans, 72000, France

Location

CHRU de Tours

Tours, 37000, France

Location

MeSH Terms

Conditions

Chest Pain

Condition Hierarchy (Ancestors)

PainNeurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and Symptoms

Central Study Contacts

Christelle JADEAU

CONTACT

Cyrielle HOUALARD, MD

CONTACT

Study Design

Study Type
observational
Observational Model
OTHER
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

February 28, 2025

First Posted

March 5, 2025

Study Start

May 2, 2025

Primary Completion

December 1, 2025

Study Completion

December 1, 2025

Last Updated

March 24, 2025

Record last verified: 2025-03

Locations