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Clinical Trials/NCT02200523
NCT02200523CompletedNot Applicable

Self Abrading Rapidly Applied (SARA) Electrode Phase II

Cleveland Medical Devices Inc2 sites in 1 country40 target enrollmentStarted: June 1, 2014Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
40
Locations
2
Primary Endpoint
Signal Quality Comparison Between SARA Electrode and Gold Cup Electrode

Study Overview

Brief Summary

The SARA (Self Abrading Rapidly Applied) electrode will speed EEG patient hookup by combining multiple steps that burden conventional EEG procedures into one. The investigators believe that the proposed system will reduce patient hookup time by more than 50% (from 40 to 20 minutes) with additional time savings on cleanup. Reducing the hookup time required for the EEG recording will make EEG more feasible in time critical situations and will improve patient care and service. The clinical testing in Phase II will investigate patient acceptance, clinician acceptance, time savings, and signal quality for 3 different environments: the large hospital institution, a small rural hospital setting and in an emergency department.

Detailed Description

The SARA (Self Abrading Rapidly Applied) electrode will speed EEG patient hookup by combining multiple steps that burden conventional EEG procedures into one. This proposed single-use electrode will consist of a Snap Top, Ag/AgCl Snap Conductor, Conductive Adhesive, and Abrader Tines in a custom molded housing and packed on a backing sheet. After removing the backing, the technician simply parts the hair with one hand and with the other hand rubs the electrode back and forth and then presses the electrode into position on the scalp. The proposed system combines the cumbersome and time-consuming skin preparation, electrode preparation and electrode fixation into one easy step. The investigators believe that the proposed system will reduce patient hookup time by more than 50% (from 40 to 20 minutes) with additional time savings on cleanup. Reducing the hookup time required for the EEG recording will make EEG more feasible in time critical situations and will improve patient care and service.

Study Design

Study Type
Interventional
Allocation
Non Randomized
Intervention Model
Parallel
Primary Purpose
Diagnostic
Masking
Single (Outcomes Assessor)

Eligibility Criteria

Ages
12 Years to — (Child, Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • adult and teenage

Exclusion Criteria

  • young children
  • damaged scalp skin
  • sensitive or allergic to electrode paste

Outcomes

Primary Outcomes

Signal Quality Comparison Between SARA Electrode and Gold Cup Electrode

Time Frame: up to 1 hour

The time it takes in seconds to properly place the SARA electrodes and standard gold cup electrodes will be recorded and compared.

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
Cleveland Medical Devices Inc
Sponsor Class
Industry
Responsible Party
Sponsor

Study Sites (2)

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