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To assess the clinical performance of CEREBO in detecting intracranial injuries in Brain Injury Patients

Comprehensive Assessment of CEREBO to evaluate its clinical performance, utility and Usability in the Brain Injury Management - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2024/07/070978
Enrollment
119
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: NIL: NIL Control Intervention1: NIL: NIL

Sponsors

Indian Council of Medical Research (ICMR)
Lead Sponsor
Bioscan Research Pvt Ltd
Collaborator

Eligibility

Inclusion criteria

Inclusion criteria: All patients with a suspected head injury and referred for head CT/MRI scan

Exclusion criteria

Exclusion criteria: Patients with scalp bruises or hematoma.

Design outcomes

Primary

MeasureTime frame
Sensitivity, Specificity, Accuracy and other clinical parameters of CEREBO in detecting intracranial injury in TBITimepoint: 3 years

Secondary

MeasureTime frame
To assess the usability of CEREBO® among healthcare professionals through survey questionnaires.Timepoint: 3 years;To evaluate the number of referrals of TBI patients from peripheral hospitals that could have been preventedTimepoint: 3 years

Countries

India

Contacts

Public ContactDr Zahir Quazi

Datta Meghe Institute of Higher Education & Research

zahirquazi@gmail.com9765404065

Outcome results

None listed

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