Motor Deficits and Signal Conduction in Individuals With Williams Syndrome

NCT05430763 · Status: WITHDRAWN · Type: OBSERVATIONAL

Last updated 2024-06-25

No results posted yet for this study

Summary

The current study aims to validate basic research findings of abnormal conductivity and motor abilities from a mouse model in humans. The study will measure nerve conduction properties in WS individuals and characterize motor symptoms in individuals with WS.

Conditions

  • Williams Syndrome

Sponsors & Collaborators

  • Tel Aviv University

    collaborator OTHER
  • Sheba Medical Center

    lead OTHER_GOV

Eligibility

Min Age
3 Years
Max Age
30 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-02-28
Primary Completion
2030-08-31
Completion
2030-08-31

Countries

  • Israel

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05430763 on ClinicalTrials.gov