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Assessment of Tele-expertise for the Interpretation of MRI Among Neonates With High Risk of Neurological Sequelae

Assessment of Tele-expertise for the Interpretation of MRI Among Neonates With High Risk of Neurological Sequelae

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03706651
Acronym
Matrix Neonat
Enrollment
70
Registered
2018-10-16
Start date
2014-01-31
Completion date
2018-01-31
Last updated
2018-10-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hypoxia, Brain

Brief summary

The purpose of the study is to determine whether tele-expertise would be more effective and more cost-effective for the Interpretation of MRI Among Neonates with high risk of neurological sequelae

Interventions

Sponsors

Agence Regionale de Sante d'Ile de France
CollaboratorOTHER_GOV
Assistance Publique - Hôpitaux de Paris
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
No minimum to 28 Days
Healthy volunteers
No

Inclusion criteria

* Less than 28 days of life * Mandatory to have a medical advice in paediatric neuroradiology for interpretation of brain MRI

Exclusion criteria

* None

Design outcomes

Primary

MeasureTime frameDescription
Time between MRI and decision of intensive care continuation1 week after dischargeA cerebral MRI for neonates, prescribed by the ICU team, will be performed, requiring a specialist advice. This advice is mandatory for ICU team to decide the intensive care continuation.

Secondary

MeasureTime frame
Time between MRI and the specialist report1 week after discharge
Time between MRI and the discussions with the parents1 week after discharge

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026