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Resting state functional MRI in term neonates with perinatal asphyxia

Resting state functional MRI in term neonates with perinatal asphyxia - NEOREST

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON44127
Enrollment
30
Registered
2013-08-06
Start date
2014-02-10
Completion date
Unknown
Last updated
2024-04-29

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

Conditions

asphyxia cerebral damage

Interventions

None listed

Sponsors

Academisch Medisch Centrum
Lead Sponsor

Eligibility

Age
2 Years to 11 Years

Inclusion criteria

Inclusion criteria: Term neonates clinically diagnosed with perinatal asphyxia.

Exclusion criteria

Exclusion criteria: Lack of informed consent of parents (parental refusal or unable to explain because of language barrier). Neonate with known congenital malformation(s) of the brain or congenital infection of the brain. Neonate with known syndrome (e.g. Down syndrome). Neonate with known congenital neuromuscular disease.

Design outcomes

Primary

MeasureTime frame
1.Feasibility of the rs-fMRI technique will be determined by assessing the image quality of the dynamic scans, the presence of motion artefacts and the temporal SNR. 2. The intra-session reproducibility of the rs-fMRI technique in neonates with asphyxia determined by the mean and Standard Deviation (SD) of the difference between 2 rs-fMRI acquisitions of 6 minutes each of the volume of the activated set of voxels and of the signal intensity of these voxels. Bland-Altman plots and Smallest Detectable Change will be used to report this.

Secondary

MeasureTime frame
nvt

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)