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Comparing MRI to CT on Pediatric Craniosynostosis.

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Mayo Clinic

Status

Completed

Conditions

Craniosynostosis

Treatments

Diagnostic Test: Zero Echo Time Magnetic Resonance Imaging (ZTE MRI)

Study type

Interventional

Funder types

Other

Identifiers

NCT04704284
19-007373

Details and patient eligibility

About

The purpose of this study is to develop and test the effectiveness and diagnostic quality of Zero Echo Time Magnetic Resonance Imaging (ZTE MRI) in comparison to CT.

Enrollment

12 patients

Sex

All

Ages

Under 18 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Pediatric patients 0-18 of age will be recruited by our surgical colleagues based on the clinical concern for craniosynostosis and possible need for calvarial reconstruction.

Exclusion criteria

  • Lack of consent
  • Contraindication/inability to undergo both examinations within the designated time period and/or undiagnostic image quality.

Trial design

Primary purpose

Other

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

12 participants in 1 patient group

ZTE MRI Imaging
Experimental group
Description:
Pediatric patients that have gotten a clinically indicated CT within a 6 week time period will receive a Zero Echo Time Magnetic Resonance Imaging (ZTE MRI)
Treatment:
Diagnostic Test: Zero Echo Time Magnetic Resonance Imaging (ZTE MRI)

Trial documents
1

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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