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NCT05340114

Usability Study of CEREBO® - A Novel Non-invasive Intracranial Bleed Detector

Status unknown NA Last updated 21 April 2022
What this trial tests

NA trial testing CEREBO® in Traumatic Brain Injury in 10 participants. Status unknown.

Timeline
25 April 2022
Primary endpoint
30 April 2023
31 May 2023

Quick facts

Lead sponsorBioscan Research Pvt. Ltd.
PhaseNA
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposedevice feasibility
Enrollment10
Start date25 April 2022
Primary completion30 April 2023
Estimated completion31 May 2023

Drugs / interventions tested

Conditions studied

Sponsor

Bioscan Research Pvt. Ltd.

Who can join

18 and older, any sex, with Traumatic Brain Injury or Intracranial Hemorrhages. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Traumatic Brain Injury (TBI) is the leading cause of death and disability across the globe. Time from injury to treatment is the most critical factor that determines the patient's recovery. Mild TBI with no apparent symptoms are often left undiagnosed, thus delaying the treatment and hence recovery. CEREBO® is a non-invasive, rapid, near-infrared based, point-of-care device that can detect an intracranial bleed at an early stage.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of CEREBO®

Trials testing the same drug.

Other recruiting trials for Traumatic Brain Injury

Currently open trials in the same condition.

Other Bioscan Research Pvt. Ltd. trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05340114.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing