COMPLETED

Non-Invasive Monitoring of Traumatic Brain Injury Progression Using the Infrascanner (MOBI-1)

Conditions

Brain Injuries, Traumatic traumatic brain injury, TBI, intracranial hematoma, ICH

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Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

MOBI-1 is a multicenter clinical trial that will evaluate the use of the Infrascanner for the monitoring of traumatic intracranial hematomas.

Official Title

Non-Invasive Monitoring of Traumatic Brain Injury Progression Using the Infrascanner (MOBI-1)

Quick Facts

Study Start:2022-04-18

Study Completion:2025-08-25

Study Type:Not specified

Phase:Not Applicable

Enrollment:Not specified

Status:COMPLETED

Study ID

NCT04893837

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:15 Years

Sexes Eligible for Study:ALL

Accepts Healthy Volunteers:No

Standard Ages:CHILD, ADULT, OLDER_ADULT

Inclusion Criteria	Exclusion Criteria
1. Age 15 or older 2. Admission CT Scan shows intracranial hemorrhage 3. Glasgow Coma Scale less than 15 4. Neurosurgery service determines initial care is nonoperative 5. Admitted for observation for TBI, to either step-down unit or intensive care unit	1. Inability to provide informed consent or lack of a legally authorized representative (LAR) 2. Admitted and observed for \>2 hours prior to screening (i.e., has already received second neurological check) 3. Other injuries deemed non-survivable 4. Diagnosed with hemorrhagic shock or receives a large volume transfusion (\>3 units of any blood product within any 1 hour) 5. Planned surgical interventions/ procedures during study period (before the second CT scan) 6. Known prisoner

Inclusion Criteria

Exclusion Criteria

1. Age 15 or older
2. Admission CT Scan shows intracranial hemorrhage
3. Glasgow Coma Scale less than 15
4. Neurosurgery service determines initial care is nonoperative
5. Admitted for observation for TBI, to either step-down unit or intensive care unit

1. Inability to provide informed consent or lack of a legally authorized representative (LAR)
2. Admitted and observed for \>2 hours prior to screening (i.e., has already received second neurological check)
3. Other injuries deemed non-survivable
4. Diagnosed with hemorrhagic shock or receives a large volume transfusion (\>3 units of any blood product within any 1 hour)
5. Planned surgical interventions/ procedures during study period (before the second CT scan)
6. Known prisoner

Contacts and Locations

Principal Investigator

Jan O Jansen, MBBS, PhD

PRINCIPAL_INVESTIGATOR

University of Alabama at Birmingham, Center for Injury Science

Study Locations (Sites)

UAB Hospital

Birmingham, Alabama, 35233

United States

University of Arizona

Tucson, Arizona, 85724

United States

Collaborators and Investigators

Sponsor: University of Alabama at Birmingham

Jan O Jansen, MBBS, PhD, PRINCIPAL_INVESTIGATOR, University of Alabama at Birmingham, Center for Injury Science

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2022-04-18

Study Completion Date2025-08-25

Study Record Updates

Study Start Date2022-04-18

Study Completion Date2025-08-25

Terms related to this study

Keywords Provided by Researchers

traumatic brain injury, TBI, intracranial hematoma, ICH

Additional Relevant MeSH Terms

Brain Injuries, Traumatic