NCT07138768

Brief Summary

This study aims to evaluate the role of stroke protocol in the early diagnosis and management of acute stroke and its effect on turnaround time (TAT) in emergency settings.

Trial Health

77
On Track

Trial Health Score

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

Enrollment
136

participants targeted

Target at P50-P75 for all trials

Timeline
7mo left

Started Aug 2025

Geographic Reach
1 country

1 active site

Status
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

Study Progress55%
Aug 2025Dec 2026

First Submitted

Initial submission to the registry

August 17, 2025

Completed
6 days until next milestone

Study Start

First participant enrolled

August 23, 2025

Completed
1 day until next milestone

First Posted

Study publicly available on registry

August 24, 2025

Completed
1.3 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 1, 2026

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2026

Last Updated

August 26, 2025

Status Verified

August 1, 2025

Enrollment Period

1.3 years

First QC Date

August 17, 2025

Last Update Submit

August 23, 2025

Conditions

Outcome Measures

Primary Outcomes (1)

  • Sensitivity of magnetic resonance imaging for acute stroke

    Sensitivity of magnetic resonance imaging for acute stroke will be recorded.

    Immediately post-procedure (Up to 1 hour)

Study Arms (1)

Study group

Patients with acute stroke who are admitted to the emergency department.

Device: Magnetic Resonance Imaging

Interventions

Magnetic Resonance Imaging will be performed to all patients

Study group

Eligibility Criteria

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

This prospective cohort study will be carried out on 136 patients presenting with acute stroke symptoms after approval from the institutional ethical committee.

You may qualify if:

  • Age ≥18 years.
  • Both sexes.
  • Patients with acute stroke who are admitted to the emergency department.

You may not qualify if:

  • Contraindications to magnetic resonance imaging (MRI) or computed tomography (CT).
  • Symptoms strongly suggestive of subarachnoid hemorrhage.
  • Initiation of antithrombotic or thrombolytic treatment before the completion of both scans.
  • Inability to complete both scans in time to allow thrombolytic treatment within three h of the onset of symptoms.
  • Uncontrollable hypertension.
  • Pregnant or lactating women.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Tanta University

Tanta, El-Gharbia, 31527, Egypt

RECRUITING

MeSH Terms

Conditions

DiseaseStroke

Interventions

Magnetic Resonance Imaging

Condition Hierarchy (Ancestors)

Pathologic ProcessesPathological Conditions, Signs and SymptomsCerebrovascular DisordersBrain DiseasesCentral Nervous System DiseasesNervous System DiseasesVascular DiseasesCardiovascular Diseases

Intervention Hierarchy (Ancestors)

TomographyDiagnostic ImagingDiagnostic Techniques and ProceduresDiagnosis

Central Study Contacts

Study Design

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

Study Record Dates

First Submitted

August 17, 2025

First Posted

August 24, 2025

Study Start

August 23, 2025

Primary Completion (Estimated)

December 1, 2026

Study Completion (Estimated)

December 1, 2026

Last Updated

August 26, 2025

Record last verified: 2025-08

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