Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
ID06149819

Nurse Pathway for the Diagnosis of Non-traumatic Chest Pain in the Emergency Department: Preliminary Pilot Study (Chest Pain Nurse Track)

Led by University Hospital, Grenoble · Updated on 2026-04-20

182

Participants Needed

1

Research Sites

21 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Chest pain is a common reason for visits to the emergency department, with causes ranging from mild issues like musculoskeletal or psychogenic pain to more serious conditions such as coronary problems. This research evaluates how safe and effective a nursing pathway is for managing patients who come to the emergency department with non-traumatic chest pain, comparing it with usual medical care. The study is interventional and aims to improve initial management by specially trained nurses following a standardized protocol. The study involves three main phases. First, emergency nurses with at least five years of experience and training receive specialized instruction on managing non-traumatic chest pain. Next, 182 patients presenting with chest pain are enrolled and assigned either to a group cared for by these trained nurses using a recommended algorithm or to a control group receiving usual medical care. Both groups are closely monitored by physicians, and an independent committee reviews the management and diagnostic compliance. Lastly, patients are followed up by phone one month after their emergency visit to record any serious events, additional tests, and overall satisfaction. Participants will be assessed through clinical examinations, electrocardiograms, chest x-rays, and ongoing physician reviews during their emergency department stay. Data will be collected on diagnosis accuracy, management timing, and patient outcomes including major cardiac events and care consumption at one month. Patient satisfaction and quality of life are also evaluated at discharge and after one month. The study includes safety oversight by a monitoring board and final analysis of diagnostic compliance to ensure thorough evaluation across both nursing and medical care groups.

CONDITIONS

Brief Title

Chest Pain Nurse Track

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Admission to emergency department for non-traumatic chest pain
  • Affiliated to the French social security system
  • Written informed consent obtained
  • For women of childbearing age: effective contraception for at least 3 months and negative pregnancy test before management
Not Eligible

You will not qualify if you...

  • Suspected alcohol, drug, or toxic intoxication
  • Chest pain with neurological signs
  • Presence of pacemaker or defibrillator
  • Vital distress needing immediate intervention
  • Previously established diagnosis for chest pain
  • Unable to communicate, non-French speaking, or impaired consciousness
  • Pregnant or breastfeeding
  • Under administrative or judicial control or protection

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Diagnostic Evaluation

Duration - Up to several hours during emergency department stay

Participants presenting with non-traumatic chest pain are evaluated in the emergency department by specially trained nurses following a standardized algorithm or by usual medical care.

1 visit (in-person during emergency department admission)

Follow-up

Duration - 1 month after emergency department discharge

Participants receive a phone call approximately one month after discharge to collect data on serious events, patient satisfaction, and any additional examinations or consultations.

1 phone call follow-up

Trial Site Locations

Total: 1 location

1

CHU Grenoble Alpes

Grenoble, Grenoble, France, 38043

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Research Team

D

Damien VIGLINO, Pr MD PhD

P

Prudence MABIALA MAKELE, PhD

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NON_RANDOMIZED

Model

PARALLEL

Primary Purpose

DIAGNOSTIC

Number of Arms

2

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