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Not Yet RecruitingNCT07231315

INTERACT4 Expansion - Validation Study

INTEnsive Ambulance-delivered Blood Pressure Reduction in Biomarker-identified Hyper-ACute Intracerebral Haemorrhage Trial - Validation Study

Status
Not Yet Recruiting
Phase
Study type
Observational
Enrollment
465 (estimated)
Sponsor
The George Institute · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

As an investigator-initiated and conducted, multi-centre, open-label, single-arm prospective observational trial, INTERACT4 Expansion aims to evaluate the diagnostic accuracy of GFAP measured using a point-of-care device, for identifying ICH in participants presenting with acute stroke-like symptoms in the pre-hospital setting compared with imaging-confirmed ICH.

Conditions

Interventions

TypeNameDescription
DIAGNOSTIC_TESTLVOneLVOne is an in vitro diagnostic rapid lateral flow chromatographic immunoassay kit

Timeline

Start date
2026-02-01
Primary completion
2026-11-01
Completion
2027-06-01
First posted
2025-11-17
Last updated
2025-11-19

Locations

4 sites across 1 country: Australia

Source: ClinicalTrials.gov record NCT07231315. Inclusion in this directory is not an endorsement.

INTERACT4 Expansion - Validation Study (NCT07231315) · Clinical Trials Directory