Under construction – not a live service
Sign in
Taking people in United KingdomNo phase

Long-Term Follow-Up of Focused Ultrasound Thalamotomy for Parkinson's Tremor

Tracks long-term safety and results of a focused ultrasound brain procedure for severe Parkinson's tremor.

Plain-language title generated from the registry record
Registry title: A Post-Approval Registry for Exablate 4000 Type 1.0 and Type 1.1 for Unilateral Thalamotomy for the Treatment of Medication-Refractory Tremor Dominant Idiopathic Parkinson's Disease

Key facts

Where
Dundee, United KingdomSee the site

Could this be for you?

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 30 and 99 years old?

Source: NCT04991831, who can take part

Where in United Kingdom

  • University of DundeeDundee, United KingdomTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
Print a page for my doctor

Trial details

Who runs it
InSightec
Trial code
NCT04991831
Record updated
20 March 2026
Original description
The objectives of this study are to collect the long-term safety and effectiveness data of performing thalamotomy for tremor dominant Parkinson's Disease (TDPD) using the Exablate Neuro system.Read full original descriptionShow less

A Post-Approval Registry for Exablate 4000 Type 1.0 and Type 1.1 for Unilateral Thalamotomy for the Treatment of Medication-Refractory Tremor Dominant Idiopathic Parkinson's Disease

The objectives of this study are to collect the long-term safety and effectiveness data of performing thalamotomy for tremor dominant Parkinson's Disease (TDPD) using the Exablate Neuro system.

Inclusion: Men and women, age 30 years and older; Subject undergoing an Exablate procedure for their planned TDPD treatment; per local institution standard of care; Subject is willing to cooperate with the Registry requirements including compliance with the regimen and completion of all study visits; Subject has signed and received a copy of the approved informed consent form.

Exclusion: Subject does not agree to participate or is unlikely to participate for the entirety of the study.

ClinicalTrials.gov NCT04991831