Bilateral Essential Tremor Treatment With Gamma Knife

Who is this study for? Patients with bilateral essential tremor
What treatments are being studied? Gamma Knife VIM thalamotomy
Status: Recruiting
Location: See all (2) locations...
Intervention Type: Procedure
Study Type: Interventional
Study Phase: Phase 2/Phase 3
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.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Patients must be ≥ 18 years

• The patient has a primary diagnosis of ET or ET plus confirmed by a movement disorder neurologist;

• The patient previously underwent a GK thalamotomy (\> 12 months ago);

• The tremor on the untreated side negatively impacts the patients' quality of life;

• The patient wants treatment of the contralateral side.

Locations
Other Locations
Canada
CIUSSS de l'Estrie-CHUS - Hôpital Fleurimont
RECRUITING
Sherbrooke
Toronto Western Hospital, University Health Network
RECRUITING
Toronto
Contact Information
Primary
Christian Iorio-Morin
christian.iorio-morin@usherbrooke.ca
819-346-1110
Time Frame
Start Date: 2021-06-08
Estimated Completion Date: 2026-10
Participants
Target number of participants: 50
Treatments
Experimental: Treatment group
Participants will undergo a thalamotomy contralateral to their previous treatment with Gamma Knife using a frame-based, Gamma Knife Perfexion or Icon unit (Elekta, Stockholm, Sweden).
Sponsors
Leads: Université de Sherbrooke
Collaborators: University Health Network, Toronto

This content was sourced from clinicaltrials.gov