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Clinical Trials in India / NCT07844109
Starting soon Not applicable

Glial Fibrillary Acidic Protein Testing and Handheld Near Infrared Spectroscopy Technology CEREBO in India.

NCT07844109 · tracked via the Priya Life Science India tracker
Phase
Not applicable
Started
2027-09-01
Last updated
2026-09-28

Condition(s) studied

Stroke

Investigational drug(s) / intervention(s)

GFAP/D-Dimer Point-of-Care Testing & CEREBO Near-Infrared Spectroscopy (NIRS)CT Head

GFAP/D-Dimer Point-of-Care Testing & CEREBO Near-Infrared Spectroscopy (NIRS): A finger-prick blood sample will be obtained from patients with suspected acute stroke and tested using a GFAP/D-Dimer lateral flow assay. The test will provide rapid biomarker results to support differentiation between ischemic stroke and intracerebral hemorrhage in the prehospital setting and The handheld CEREBO-NIRS device will be applied non-invasively to the patient's scalp to detect intracranial hematoma by assessing asymmetry in near-infrared optical density. The findings will be recorded and used as part of the PREDICT Assessment Model for stroke subtype classification.

CT Head: Standard care CT head imaging

Study summary

CEREBO is an ICMR award winning point-of-care (POC) adjunct CT scanning device for detecting brain hematomas in patients with head injury. The study aims to validate the diagnostic accuracy of the PREDICT Assessment Model (CEREBO-NIRS plus GFAP/D-Dimer POC Assay) in patients with suspected stroke. The study will be conducted as part of the Indian Council of Medical Research's National Health Research Priority (ICMR-NHRP) under the INDIA-EMS project using a two phase design.

PHASE I: Validation of a diagnostic accuracy and feasbility of PREDICT assessment model (a combined approach using GFAP/ D-dimer POC lateral flow assay plus CEREBO-NIRS technology).

Study Design: Prospective, Multicenter, Validation and Feasibility Study.

PHASE II: Pilot RCT to assess integration of the PREDICT assessment model into pre-hospital pathways.

Study Design: Pilot Randomized Controlled Trial (RCT) (Year 3-5)

Eligibility

Sex
ALL
Min age
18 Years
Max age
99 Years
Healthy volunteers
No
Phase 1 Inclusion criteria * Adult patients of any gender ≥18 years with clinically suspected stroke * Transported by ambulance or presenting directly to ED of participating hospitals * Time from symptom onset/ Lost known well time (within 24 hours) * Consent provided by patient/ next of kin Exclusion criteria: * Patients with known pre-existing neurological conditions that may confound diagnosis (Concurrent traumatic brain injury, recent TBI in last 3months, IS/ICH in last 3 months, Diagnosis of brain tumour/SOL) * Patients with known medical condition with estimated life expectancy ≤ 3 months * Those refusing consent Phase 2 Inclusion criteria: * Adult patients of any gender ≥18 years with clinically suspected stroke * Transported by ambulance to ED of participating hospitals * Time from symptom onset/ Last well known time (≤ 24 hours) * NIHSS ≥ 5 * Consent provided by patient/ next of kin Exclusion criteria: * Patients with known pre-existing neurological conditions that may confound diagnosis (Concurrent traumatic brain injury, recent TBI in last 3months, IS/ ICH in last 3 months, Diagnosis of brain tumour/ SOL) * Patients with known medical condition with estimated life expectancy ≤ 3 months * Those refusing consent

Primary outcome measure(s)

Trial sites (2)

FacilityCityRegionStatus
Jawaharlal Institute of Postgraduate Medical Education and Research Puducherry JIPMER Puducherry Puducherry
Christian Medical College and Hospital Ludhiana Punjab

More Christian Medical College and Hospital, Ludhiana, India trials in India

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07844109 on ClinicalTrials.gov ↗ ← All trials in India