Skip to content
Trial Eligibility
Menu

A Post-Approval Registry for Exablate 4000 Type 1.0 and Type 1.1 for Unilateral Pallidotomy for the Treatment of Advanced, Idiopathic Parkinson's Disease With Medication-refractory Moderate to Severe Motor Complications

NCT05539196

This study is recruiting at 4 US sites in 4 states, according to its ClinicalTrials.gov record last updated .

Summary

This registry is a prospective, multicenter, international, single arm, observational post-approval registry with follow-up at 3, 6, and 12 months, and annually for 5 years. The proposed registry will enroll 60 subjects and will be conducted at approximately 10 centers worldwide.

Shortened from the sponsor's brief summary. View official record on ClinicalTrials.gov

Conditions studied

  • Movement Disorders
  • Neurology
  • Parkinsons Disease

Eligibility basics and study details

Study type
Observational
Phase
Not applicable
Ages
30 to 99 years
Sex
All
Healthy volunteers
Not accepted
Sponsor
InSightec
Last updated on ClinicalTrials.gov
March 20, 2026

These are the basic criteria only. The full inclusion and exclusion criteria are on the official record, and the study team decides who can take part.

US recruiting sites

Maryland · 1

  • University of Maryland, Baltimore · Baltimore, MD

New York · 1

  • Weill Cornell Medicine · New York, NY

Pennsylvania · 1

  • University of Pennsylvania · Philadelphia, PA

Texas · 1

  • University of Texas Southwestern Medical Center · Dallas, TX

Source: ClinicalTrials.gov, data processed . Recruiting US sites filtered by distance and site status; summaries shortened.