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Clinical Trials/NCT01602042
NCT01602042
Completed
N/A

Phase II Study: Adaptive Portable Essential Tremor Monitor

Great Lakes NeuroTechnologies Inc.2 sites in 1 country20 target enrollmentMay 2012

Overview

Phase
N/A
Intervention
Not specified
Conditions
Essential Tremor
Sponsor
Great Lakes NeuroTechnologies Inc.
Enrollment
20
Locations
2
Primary Endpoint
Tremor ratings during activities of daily living versus standardized tasks.
Status
Completed
Last Updated
13 years ago

Overview

Brief Summary

The purpose of this study is to evaluate the utility of a portable motion sensor-based system designed to monitor essential tremor (ET) to better prescribe therapy to minimize symptoms and expand care for ET patients.

Registry
clinicaltrials.gov
Start Date
May 2012
End Date
November 2012
Last Updated
13 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Aged 18 years or older
  • Clinical diagnosis of essential tremor
  • Able to provide informed consent

Exclusion Criteria

  • Significant medical or psychiatric illness
  • Not capable of following the required clinical instructions
  • Serious medical conditions that compromise safety

Outcomes

Primary Outcomes

Tremor ratings during activities of daily living versus standardized tasks.

Time Frame: 10 hours each day the sensor is worn.

Study Sites (2)

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