To evaluate the performance of near infrared-based device in the management of traumatic brain injury patients.

Feasibility Assessment of CEREBO? in conjunction with CEREBO? Research Unit (CCRU)to detect structural and functional injury among brain injury patients - NIL

Status

Active, not recruiting

Phases

Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2024/01/062065

Enrollment

180

Registered

2024-01-30

Start date

Unknown

Completion date

Unknown

Last updated

2024-03-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: S068- Other specified intracranial injuries

Interventions

Intervention1: Near infrared based Device: Participants will be randomly allocated to the experimental and the control group. The experimental group would receive an additional scan using the CCRU dev

Eligibility

Inclusion criteria

Inclusion criteria: 1. Traumatic and non-traumatic patients who are referred for a head CT or an MRI scan. 2. Suspected CVA or infarct

Exclusion criteria

Exclusion criteria: 1. History of neurosurgical procedure (e.g. decompressive craniectomy) with residual bone flap. 2. Post-Operative patients.

Design outcomes

Primary

Measure	Time frame
To assess the structural and functional injury in traumatic brain injury patientsTimepoint: 3 years	—

Secondary

Measure	Time frame
Reduction in the mean transfer time from injury to first head CT ScanTimepoint: 3 years	—

Countries

India

Contacts

Public ContactDr Vijaya Sekhar M V

Government General Hospital

nsvijayasekhar@gmail.com9849115723

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026