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NCT05521217

Myotonometer Intra- and Inter Examiner Reliability on Spinal Muscular Atrophy

Status unknown Last updated 25 October 2022
What this trial tests

trial testing MyotonPRO in Muscle Tone Poor in 30 participants. Status unknown.

Timeline
26 August 2022
Primary endpoint
15 October 2022
15 October 2022

Quick facts

Lead sponsorIstanbul Medipol University Hospital
StatusStatus unknown
Study typeOBSERVATIONAL
Enrollment30
Start date26 August 2022
Primary completion15 October 2022
Estimated completion15 October 2022
Sites2 locations across Turkey (Türkiye)

Drugs / interventions tested

Conditions studied

Sponsor

Istanbul Medipol University Hospital

Who can join

Adults 1 Month to 4, any sex, with Muscle Tone Poor or Spinal Muscular Atrophy. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The primary aim of the study was to measure the intra-rater and inter-rater reliability of MyotonPRO in measuring postural muscle tone and mechanical properties in individuals with spinal muscular atrophy (SMA). The secondary aim is to question the existence of a relationship between the functional levels of individuals with SMA and their muscle tone and biomechanical properties. It is assumed that the outputs to be obtained from this research will form the norm data for moyotonometer evaluation in children with SMA.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Intersession Intra-Rater and Inter-Rater Reliability of Myotonometer for Upper and Lower Extremity Muscles in Children with Spinal Muscular Atrophy.
    Kutlutürk Yıkılmaz S, Çevik Saldıran T, Öztürk Ö, Öktem S. · · 2024 · cited 1× · PMID 39451623 · DOI 10.3390/diagnostics14202300

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Other trials of MyotonPRO

Trials testing the same drug.

Other Istanbul Medipol University Hospital trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05521217.

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