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OpenTrials
Completed

NCT Number: NCT06204575

Focused Ultrasound Thalamotomy for Tremor Relief in Atypical Parkinsonism

The goal of this retrospective observational study is to describe the efficacy of focused ultrasound ventral-intermediate nucleus thalamotomy in patients with atypical parkinsonism.

* Is this treatment efficacious in patients with multiple system atrophy? * Is this treatment efficacious in patients with diffuse Lewy Body Dementia? Data will be collected from patients charts.

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Key information

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion Patients that underwent FUS ventral-intermediate nucleus thalamotomy Suffer from multiple system atrophy-Parkinsonian type (MSA-P) or dementia with Lewy bodies (DLBD).

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Exclusion criteria

  • Patients that did not underwent FUS ventral-intermediate nucleus thalamotomy
  • Patients that underwent FUS ventral-intermediate nucleus thalamotomy and do not suffer from MSA or DLBD

Treatment and study plan

Data Collection

Other

Data collection

Primary outcomes

  1. Clinical Rating Scale for Tremor

    Time frame: baseline, pre-procedure, 1 month, 6 months and 1 year following procedure

    tremor assessment by Clinical Rating Scale for Tremor. Scores ranging from 0 to 156, with higher scores indicating more severe tremor.

Sponsors and collaborators

Lead sponsor

Rambam Health Care Campus

Other

Registry information

Acronym: FUSAP

Important dates

Study start
2013
Primary completion
2023
Study completion
2023
First posted
Jan 12, 2024
Registry last updated
Jan 12, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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