Clinical Trials Directory

Trials / Recruiting

RecruitingNCT04748640

Bilateral Essential Tremor Treatment With Gamma Knife

Status
Recruiting
Phase
Phase 2 / Phase 3
Study type
Interventional
Enrollment
50 (estimated)
Sponsor
Université de Sherbrooke · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

Combined Phase II/III, multi-center, prospective, single-blinded trial. Ten (10) patients with essential tremor who previously underwent successful and uncomplicated GK thalamotomy for essential tremor will undergo a contralateral treatment. The incidence of side effects will be determined at 3 months postoperatively, graded per the CTCAE v5 and analyzed by a data safety monitoring board. Upon successful review, this Phase II trial will be converted to a Phase III trial of utility that will enrol 40 additional patients. The primary outcome will be the change in QUEST score at 12 months postoperatively, as well as a patient-reported assessment of Health Utility. Secondary outcomes will include objective tremor, gait and speech assessments (filmed and scored by blinded evaluators), as well as quality of life questionnaires and adverse events questionnaires. Outcomes will be assessed at baseline, as well as 3, 6, 12, 24 and 36 months post-operatively.

Conditions

Interventions

TypeNameDescription
PROCEDUREGamma Knife VIM thalamotomyAblation of contralateral VIM nucleus of thalamus with GK using a frame-based, Gamma Knife Perfexion or Icon unit (Elekta, Stockholm, Sweden).

Timeline

Start date
2021-06-08
Primary completion
2026-02-01
Completion
2026-10-01
First posted
2021-02-10
Last updated
2021-11-17

Locations

2 sites across 1 country: Canada

Source: ClinicalTrials.gov record NCT04748640. Inclusion in this directory is not an endorsement.