Continuous mONitoring of recovery iN acutE isChaemic sTroke (CONNECT) - Phase 2

Not Applicable

• Conditions: Acute Ischaemic Stroke (AIS); Neurological - Other neurological disorders; Stroke - Ischaemic

• Registration Number: ACTRN12622001486718
• Lead Sponsor: The George Institute

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2022-11-28
• Last Update Posted: 15 January 2024

Recruitment & Eligibility

• Status: ot yet recruiting
• Sex: All
• Target Recruitment: 260

Inclusion Criteria

1.Adults (age >= 18 years);
2.AIS (initial diagnostic scan within 24 hours from symptom onset or last known well time) in anterior circulation due to large vessel occlusion (LVO, occlusion at the internal carotid artery, the middle cerebral artery horizontal or insular segment, or proximal site of the anterior cerebral artery), diagnosed by clinician and confirmed on CT with/without angiography;
3.At least moderate neurological severity (National Institute of Health Stroke Scale [NIHSS] score >4); and
4.Provision of consent.

Exclusion Criteria

1.Recent (<1 months) brain surgery;
2.Evidence of seizure activity from stroke symptom onset to study inclusion;
3.Having history of severe skin rash due to ECG/EEG electrode patches;
4.Skin conditions on scalp or face that preclude safe use of the device (local infections, rashes, fragile skin, etc.);
5.Having difficulties to wear the device stably (e.g., patients with severe dementia, extreme agitation, or susceptible to stress).
6. Inability to communicate in English either personally or through translator

Study & Design

• Study Type: Interventional
• Study Design: Not specified