Trials / Unknown
UnknownNCT02310282
Telemedicine for Optimized Collection of CLinical datA in Patients With Suspicion of Acute Stroke
- Status
- Unknown
- Phase
- —
- Study type
- Observational
- Enrollment
- 50 (estimated)
- Sponsor
- Universitair Ziekenhuis Brussel · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
Observational prospective single-center study on the discriminatory value of the Unassisted TeleStroke Scale for differentiation between patients with lacunar stroke and those with other acute stroke syndromes.
Detailed description
Assessment of stroke severity and differentiation between large-artery and small-artery stroke is pivotal for adequate treatment decision taking. Patients with small vessel stroke tend have a better prognosis than those with large artery disease. Further, patients with small artery infarction (lacunar stroke) have shown to respond well to treatment with intravenous recombinant tissue plasminogen activator (IV rt-PA), but are poor candidates for endovascular recanalization. Conversely, IV rt-PA may be less effective at restoring perfusion of large artery occlusion, a stroke subtype that may benefit from intra-arterial thrombolysis or embolectomy. Similarly, patients with large intracerebral hemorrhage or cerebellar hemorrhage may require neurosurgical interventions, such as intracranial pressure monitoring, ventricular drainage, surgical evacuation, or hemicraniectomy. The purpose of TeleCLASS is to evaluate the discriminatory value of the Unassisted TeleStroke Scale (UTSS) obtained through in-hospital telemedicine for differentiation between patients with lacunar stroke and those with other acute stroke syndromes (nonLACS).
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Telemedicine | In-hospital telemedicine |
Timeline
- Start date
- 2014-11-01
- Primary completion
- 2017-01-01
- Completion
- 2017-01-01
- First posted
- 2014-12-08
- Last updated
- 2016-10-28
Locations
1 site across 1 country: Belgium
Source: ClinicalTrials.gov record NCT02310282. Inclusion in this directory is not an endorsement.