Evaluating the clinical effectiveness of CEREBO in traumatic brain injury management

Investigating the Clinical Efficacy of CEREBO for early detection of Traumatic Brain Injury - NIL

Status

Active, not recruiting

Phases

Phase 4

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2024/07/071021

Enrollment

198

Registered

2024-07-22

Start date

Unknown

Completion date

Unknown

Last updated

2024-08-19

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: CEREBO: Participants in the experimental group will undergo a one-time scan with the CEREBO device prior to receiving their standard care during triaging. The scanning process is brief,

Eligibility

Inclusion criteria

Inclusion criteria: Traumatic brain injury patients arriving at the emergency department and referred for a head CT scan

Exclusion criteria

Exclusion criteria: History of neurosurgical procedure (e.g. decompressive craniectomy) with residual bone flap

Design outcomes

Primary

Measure	Time frame
To evaluate the triaging efficacy of CEREBO® by calculating the 1. Sensitivity 2. Specificity 3. Accuracy 4. Positive Predictive Value 5. Negative Predictive ValueTimepoint: 3 years	—

Secondary

Measure	Time frame
To assess the usability of CEREBO® among healthcare professionals through survey questionnairesTimepoint: 3 years;To evaluate the utility of CEREBO® in reducing the mean transfer time from triage to treatmentTimepoint: 3 years	—

Countries

India

Contacts

Public ContactDr Vedang Mahajan

All India Institute of Medical Sciences, Delhi

skale67@gmail.com9811426806

Outcome results

None listed

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