ClinicalTrials.gg
RecruitingNCT07339787DAITSUUpdated Jan 14, 2026

Diagnosis of Transient Ischemic Attacks in the Emergency Department

An observational study in Transient Ischemic Attack and Cardiovascular Morbidity, sponsored by University Hospital, Strasbourg, France. Recruiting at 1 site in France. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-01-14.

Sponsored by University Hospital, Strasbourg, France · Observational

From the registry’s dates

  • Started Feb 2025; still recruiting 1 year 9 months later.
Study type
Observational
Model
Case-only
Time perspective
Retrospective
Enrollment
300
Ages
18 Years and older
Sex
All
01

Study summary

Patients presenting a Transient Ischemic Attack (TIA) and admitted to the Emergency Department should be referred to a neurovascular specialist. In recent years, several hospitals have established TIA clinics. These units are day hospitals where all the necessary examinations are performed. Access to this expertise has proven beneficial in reducing cardiovascular morbidity and mortality, particularly the risk of early recurrence. Unfortunately, this access is limited by issues of medical demographics and unequal access to the healthcare system. In practice, this ideal care is not always possible. A portion of the TIA population is at low risk, and diagnostic and therapeutic interventions are limited, not always requiring neurovascular expertise.

The hypothesis of this research is that the management of a patient who has suffered a TIA (additional examinations, treatment, referral) is not linked to their cardiovascular risk and that the performance of additional examinations and therapies is incomplete.

02

Conditions studied

  • Transient Ischemic Attack
  • Cardiovascular Morbidity

Keywords

  • Transient Ischemic Attack
  • Cardiovascular Morbidity
03

In context

Ischemic Attack, Transient

329 studies on the registry are indexed under Ischemic Attack, Transient; 71 are open to participants now.

This study's planned enrollment of 300 is below the median of 343 across 140 observational studies indexed under Ischemic Attack, Transient.

Browse Ischemic Attack, Transient studies →

Lead sponsor

University Hospital, Strasbourg, France is the lead sponsor of 999 studies on the registry; 358 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Adult (≥18 years old) having consulted the emergency department or been diagnosed with TIA during the period from January 1, 2024, to December 12, 2024 (records will be compiled via coding at the East Rescue regional emergency observatory)

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Adult (≥18 years old)
  • Having consulted the emergency department or been diagnosed with during the period from January 1, 2024, to December 12, 2024 (records will be compiled via coding at the East Rescue regional emergency observatory)
  • TIA will be defined as a sudden, transient neurological deficit that had disappeared by the time of arrival at the emergency department

Exclusion criteria

Exclusion Criteria:

- Subjects with a suspected diagnosis of , i.e., with a sudden, transient neurological deficit that had disappeared by the time of arrival at the emergency department.

Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

TIA (transient ischaemic attack)

A “mini-stroke”: temporary stroke-like symptoms caused by reduced blood flow to part of the brain, spinal cord or eye, without signs of a new stroke on a scan.

Stroke symptoms need emergency care at once, even if they go away.

05

Study design

Observational model
Case-only
Time perspective
Retrospective
Enrollment
300 participants (estimated)
Patient registry
No
06

What researchers measure

Primary outcomes

  1. ABCD2 Score

    The ABCD2 score is a medical tool used by doctors after a TIA (Transient Ischemic Attack). The total score ranges from 0 to 7: * 0-3: low risk * 4-5: moderate risk * 6-7: high risk

    Time frame: Up to 12 months

07

Study locations

1 of 1 sites recruiting
08

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Started Feb 2025 (actual). Primary completion is estimated for Jan 2027, 23 months after the start.

How these figures are worked out, and which studies are left out of them.

Registered
Jan 5, 2026
First posted
Jan 14, 2026
StartActual
Feb 6, 2025
Primary completionEst.
Jan 2027
CompletionEst.
Jan 6, 2027
Last update
Jan 14, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Jan 14, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT07339787
Responsible party
Sponsor
First posted
Jan 14, 2026
Start date
Feb 6, 2025
Primary completion
Jan 2027 (estimated)
Completion
Jan 6, 2027 (estimated)
Last update
Jan 14, 2026

Study contacts

Pierrick LE BORGNE, MD
Contact
Pierrick.LEBORGNE@chru-strasbourg.fr
33 3.88.12.86.90
Mathieu OBERLIN, MD
Contact
mathieu.oberlin@ghso.fr
33 6.72.07.23.60

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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