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Feasibility of Diffusion Tensor Imaging MRI in post-polio syndrome

Feasibility of Diffusion Tensor Imaging MRI in post-polio syndrome - DTI in PPS

Status
Unknown
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON38530
Enrollment
30
Registered
2013-04-26
Start date
Unknown
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

Post-polio syndrome

Interventions

None listed

Sponsors

Academisch Medisch Centrum
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: PPS patients: Subject has symptomatic quadriceps deterioration, evidence of enlarged motor units (as measured by high-density surface EMG) and isometric quadriceps muscle strength of >=30Nm in at least one leg. Subject has symptoms for >= 1 year that cannot be explained by any other neurological disorder Healthy controls: Subject is free of symptoms that can be explained by any neurological disorder

Exclusion criteria

Exclusion criteria: PPS patients & healthy controls: Subject is unwilling or unable to participate in this study and to give informed consent. Subject is also excluded if prosthesis registration number cannot be acquired (relatively new prostheses are not a contra-indication for MRI, this can be checked with the prosthesis registration number) (If applicable). Other exclusion criteria are contra-indications to undergo an MRI scan (pregnancy, claustrophobia, metal corpora aliena or metal implants such as pacemakers)

Design outcomes

Primary

MeasureTime frame
Main study endpoint will be a characterization of changes in DTI parameters of affected muscles, isometric muscle strength measurements (quadriceps) and a full picture of the architectural organization of lower limb muscles and the leg as a whole.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)