RECRUITING

Portable Rapid Imaging for Medical Emergencies

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Conditions

Patient SatisfactionConventional Magnetic Resonance ImagingPortable Magnetic Resonance ImagingBrain MRI

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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

This study will compare the time it takes to scan a patient in the emergency department with a portable MRI when compared to a conventional MRI. Participants will be randomized to receive a portable MRI plus standard of care (SOC) vs SOC. Investigators will look at time to beginning of scan for both.

Official Title

Portable Rapid Imaging for Medical Emergencies

Quick Facts

Study Start:2025-04-21
Study Completion:2026-04
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06930534

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:18 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Male or female ≥ 18 years of age at presentation to Yale New Haven Hospital Adult ED
  2. * Order to receive conventional brain MRI imaging originating in the YNHH Adult ED
  1. * Lack of assent from treating physician for inclusion in this protocol.
  2. * Contraindications to 1.5T MRI evaluation, including:
  3. 1. Cardiac Pacemaker or defibrillator
  4. 2. Aneurysm clip
  5. 3. Implants or devices attached to the body in the chest or above, such as:
  6. 1. Nerve stimulator
  7. 2. Deep brain stimulator
  8. 3. Programmable shunt
  9. 4. Stent
  10. 5. Pain pump
  11. 6. Artificial extremity
  12. 4. Implants in the ears (hearing aid or cochlear implant
  13. 5. Any shrapnel, pellets, bullets, metallic fragments, or other metallic foreign body above the chest
  14. 6. Metallic joints, rods, screws, or other orthopedic implants in or above the chest
  15. 7. Braces, dentures, removable teeth, or dental expanders that cannot be removed.
  16. 8. Body piercings in or above the chest that cannot be removed.
  17. 9. MRI-incompatible Tracheostomy tube or Swan Ganz catheter in place
  18. 10. History of uncontrolled seizures

Contacts and Locations

Study Contact

Adam H de Havenon, MD
CONTACT
203-785-4085
adam.dehavenon@yale.edu

Principal Investigator

Adam de Havenon, MD
PRINCIPAL_INVESTIGATOR
Yale University

Study Locations (Sites)

Yale New Haven Health Emergency Department
New Haven, Connecticut, 06520
United States

Collaborators and Investigators

Sponsor: Yale University

  • Adam de Havenon, MD, PRINCIPAL_INVESTIGATOR, Yale University

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 Date2025-04-21
Study Completion Date2026-04

Study Record Updates

Study Start Date2025-04-21
Study Completion Date2026-04

Terms related to this study

Keywords Provided by Researchers

  • Brain MRI

Additional Relevant MeSH Terms

  • Patient Satisfaction
  • Conventional Magnetic Resonance Imaging
  • Portable Magnetic Resonance Imaging