Skip to main content
OpenTrials
Completed

NCT Number: NCT04042584

Visio-conference for Pre-hospital Triage of Stroke Suspicions

Interventionnal Study to investigate the accuracy of our clinical based algorithm performed by using a visioconference device to assess the eligibility of acute recanalisation treatment (intraveinous thrombolysis (IVT) and/or mechanical thrombectomie (TM). Clinical identification of type of treatment is needed is pre-hospital triage of these patients.

Completed

Looking for future studies?

Notify Me

Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

CHU de Bordeaux

Bordeaux, 33 076, France

About this study

The outcome of ischemic stroke (IS) with large artery occlusion (LVO) is related to the volume of infarcted brain witch is related to the delay of arterial recanalisation. IVT is available in multiple stroke units in France but, in case of LVO, the association with TM is needed. The availability of endovascular capable centers is limited to tertiary care hospitals. As a result, pre-hospital identification of these patients is a priority and the optimization of the triage can be done by a clinical algorithm carried out by a neurological tele-evaluation.

OPTIC-AVC is a multi-phase study. This phase is about the evaluation of accuracy of our algorithm performed by a quick and standardized neurological tele-evaluation to predict the eligibility for recanalisation treatment (IVT and/or TM) of patients suspected of acute stroke in the emergency setting. The effective therapeutic decision for each patient, performed by another neurologist, will be blind to the theoretical therapeutic decision resulting from the algorithm.

Theoretical and effective therapeutic decision will be compared a posteriori

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age over 18
  • Suspicion of acute symptomatic stroke whose first symptoms are less than 24 hours old
  • Free Consent, informed writing signed by the participant or the person of confidence and the investigator (no later than the day of inclusion and before any examination required by research)

Exclusion criteria

  • Stupor or coma requiring orotracheal intubation
  • Rankin pre stroke > 4
  • Severe cognitive impairement
  • Contraindication to the realiszation of angiographic imaging
  • Participation refusal
  • Patient under legal protection

Treatment and study plan

Visio conference device evaluation (DVCM)

Procedure

Standard neurological tele-evaluation (limited to 15minutes) remotely carried out by a first neurologist via a tablet (DVCM) and an operator. A second neurologist assist at the assessment without intervention next to the patient. Once the remote assessment is complet, the second neurologist ensure the continuation of standard patient care.

Primary outcomes

  1. Final effective therapeutic decision

    Time frame: Day 0

    Thrombolysis and/or thrombectomy : yes/no

Secondary outcomes

  1. Therapeutic conviction

    Time frame: Day 0

    Theoretical conviction using Likert scales between the neurologist at the patient bedside and the neurologist using the device for tele-evaluation

  2. Remote evaluation failure

    Time frame: Day 0

    Remote evaluation failure rate

  3. Theoretical therapeutic decision

    Time frame: Day 0

    Theoretical therapeutic decision of the algorithm : thrombolysis and/or thrombectomy [yes/no]

Sponsors and collaborators

Lead sponsor

University Hospital, Bordeaux

Other

Registry information

Official study title

Pre-hospital Optimization of Triage of Stroke Suspicions: Bringing an Embedded Visio Conference Device

Acronym: OPTIC-AVC

Important dates

Study start
2019
Primary completion
2021
Study completion
2021
First posted
Aug 2, 2019
Registry last updated
Jun 18, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.