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
| Type | Name | Description |
|---|---|---|
| PROCEDURE | Gamma Knife VIM thalamotomy | Ablation 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.