Skip to main content
Clinical Trials/NCT00331669
NCT00331669
Unknown
Phase 2

Multicenter, Randomized Trial on the Effects of Pallidal Deep Brain Stimulation for Tardive Dystonia

Charite University, Berlin, Germany1 site in 1 country24 target enrollmentMay 2006

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
Dystonia
Sponsor
Charite University, Berlin, Germany
Enrollment
24
Locations
1
Primary Endpoint
Improvement of the motor scale of Burke-Fahn-Marsden-Dystonia Rating Scale via blinded video assessment 3 months after starting DBS in comparison to sham-stimulated patients
Last Updated
17 years ago

Overview

Brief Summary

The purpose of this randomized, double blind, multi-center study is to assess the efficacy and safety of bilateral pallidal deep brain stimulation in patients with tardive dystonia.

Detailed Description

Deep brain stimulation (DBS) has been established as a new reversible, neurosurgical therapeutic option for patients suffering from disabling neurological movement disorders such as essential tremor and Parkinson´s disease. Recently, deep brain stimulation has been successfully applied in patients with primary generalized and segmental dystonia. Additionally, a number of case reports suggest that pallidal deep brain stimulation may also improve tardive dystonia, which may for instance result from the intake of neuroleptics and which is notoriously difficult to treat medically. The present study will investigate the effects of pallidal DBS using a double blind, randomized design (sham- versus verum-stimulation within a 3-months interval post implantation of the electrodes). Initially 60 patients had been calculated in a power analysis to assess significant results based on an average improvement of dystonic symptoms of 30%. However, in a recent study (Damier et al., Archives of General Psychiatry, 2007), 10 out of 10 showed a successful outcome of approximately 50% decrease on the extrapyramidal symptoms rating scale score. The exact one- sided lower 95% confidence limit would be 0.794 for this result. If such an approach is chosen for sample size estimation with 18 verum and 18 placebo patients one would obtain a power of 82% against a placebo effect of 30% success rate. For a placebo effect of 25% one needs 16+16 patients and for the placebo effect of 20% one needs 12+12 patients. We thus decided to reduce the sample size to 36- 32- 24 patients. It is expected that the continuous primary outcome measure will preserve even higher power than the binary one used in the study mentioned above. The local ethical committee has approved this.

Registry
clinicaltrials.gov
Start Date
May 2006
End Date
December 2010
Last Updated
17 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Operational criteria for tardive dystonia for \> 18 months after cessation of neuroleptic exposure
  • 18-75 years
  • Relevant functional impairment in daily living activities
  • BFMDRS \> 8 or AIMS \> 16
  • Informed written consent

Exclusion Criteria

  • PANNS \>60 (Schizophrenia)
  • Hamilton-Score \> 18 (Depression)
  • MATTIS-Score \<120 (Dementia)
  • Preceding stereotactic neurosurgery
  • Pronounced brain atrophy
  • Increased bleeding risk
  • Decreased immune status
  • Botulinum Toxin treatment within the last 3 months

Outcomes

Primary Outcomes

Improvement of the motor scale of Burke-Fahn-Marsden-Dystonia Rating Scale via blinded video assessment 3 months after starting DBS in comparison to sham-stimulated patients

Time Frame: 3 months

Secondary Outcomes

  • AIMS(3 months)
  • Non-motor subscores of BMFDRS(3 months)
  • Visual analogue scales for both patients and treating physicians(3 months)
  • Quality of life (SF-36)(3 months)
  • Psychiatric assessment (HADS-D and PANSS)(3 months)

Study Sites (1)

Loading locations...

Similar Trials