NCT06836466

Brief Summary

This study aims to investigate physicians' awareness regarding patients presenting with potential acute ischemic chest pain. It focuses on various electrocardiogram (ECG) patterns requiring prompt catheter lab activation for reperfusion therapy alongside other ECG mimics that may lead to false catheter lab activations.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
640

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Feb 2025

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
completed

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 13, 2025

Completed
7 days until next milestone

First Posted

Study publicly available on registry

February 20, 2025

Completed
Same day until next milestone

Study Start

First participant enrolled

February 20, 2025

Completed
6 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

August 29, 2025

Completed
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

September 30, 2025

Completed
Last Updated

November 18, 2025

Status Verified

February 1, 2025

Enrollment Period

6 months

First QC Date

February 13, 2025

Last Update Submit

November 14, 2025

Conditions

Outcome Measures

Primary Outcomes (1)

  • Physicians' Awareness

    Physicians' awareness is measured by a numerical score of 0 to 10, depending on the electrocardiogram (ECG) pattern survey. 0 means (least recognition of ECG pattern) and 10 (high recognition of ECG pattern)

    At time of online survey (Up to 2 months)

Study Arms (1)

Group 1

All physicians are subjected to 10 ECGs Surves

Other: Google Form-based questionnaire

Interventions

All participants will consent to submit an anonymous Google Form-based questionnaire. The designed questionnaire includes introductory personal, academic, and work experience data about the physicians as gender, age, current specialty, workplace, highest achieved medical-academic or training degree, and number of years of postgraduate clinical work experience.

Group 1

Eligibility Criteria

Age25 Years - 65 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

A consecutive sample of 500 physicians who treat patients with possible acute ischemic chest pain will be the subject of this cross-sectional survey study. These doctors will include emergency physicians, cardiologists, internal medicine/acute medicine specialists, general practice or family physicians, anesthesiologists, and intensive care physicians of both sexes, with varying degrees of experience and post-graduate clinical training, from all over the world.

You may qualify if:

  • Age from 25 to 65 years.
  • Both sexes.
  • Physicians who treat patients with possible acute chest pain.

You may not qualify if:

  • \- Participants who failed to complete the survey questions.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Tanta University

Tanta, El-Gharbia, 31527, Egypt

Location

Study Design

Study Type
observational
Observational Model
OTHER
Time Perspective
CROSS SECTIONAL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Lecturer of Emergency and Traumatology, Faculty of Medicine, Tanta University, Tanta, Egypt.

Study Record Dates

First Submitted

February 13, 2025

First Posted

February 20, 2025

Study Start

February 20, 2025

Primary Completion

August 29, 2025

Study Completion

September 30, 2025

Last Updated

November 18, 2025

Record last verified: 2025-02

Data Sharing

IPD Sharing
Will share

The data will be available upon a reasonable request from the corresponding author after the end of study for one year.

Shared Documents
STUDY PROTOCOL
Time Frame
After the end of study for one year.
Access Criteria
The data will be available upon a reasonable request from the corresponding author.

Locations