MedPath

Verify the Performance of the Neutral Electrode (NE) Adhesives

Completed
Conditions
Adhesion of the Neutral Electrode 21pad
Interventions
Device: Medline NE Grounding Pad
Registration Number
NCT05376787
Lead Sponsor
Medline Industries
Brief Summary

The purpose of this research study is to determine the neutral electrode 21pad adhesion to the skin in accordance with international standard IEC 60601-2-2 section 201.15.101.7. A neutral electrode is placed on the body of patients undergoing surgery that involves the use of electric current, to protect them from the harmful effects of the electricity.

Detailed Description

Two neutral electrodes will be applied to the front of your thighs. The study staff will set up and attach a pulley system to the neutral electrodes. The purpose of the pulley system is to apply a force pulling the neutral electrode away from your body. The force will be applied for 10 minutes on each neutral electrode in one direction, and then for another 10 minutes in a second direction. Site staff will mark any areas of separation and the neutral electrodes will be removed.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
20
Inclusion Criteria
  • Participants must be willing to comply with all study procedures
  • Participants must be willing to shave, or to have shaved, the sites where the neutral electrodes will be placed.
Exclusion Criteria
  • The participant has any skin conditions (e.g. eczema, sensitivities, allergies to adhesives, sunburn, etc.) at the application sites that might be adversely affected by the application of an adhesive pad.
  • The participant is pregnant or breastfeeding.

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
Healthy SubjectsMedline NE Grounding PadSubjects must be 18 years old or over, willing to shave or have shaved the sites where the neutral electrodes will be placed. Subjects also must not be pregnant, breastfeeding, have skin conditions (such as eczema, sensitivities, allergies to adhesives, sunburn).
Primary Outcome Measures
NameTimeMethod
Number of Tests With No More Than 5% Separation - Neutral Electrode (NE) Adhesive SeparationUp to 20 minutes - (10 minutes w. Pull for 10 to 10.25 minutes, in a plane parallel to the NE pad & At 10 mins, change direction of pull to y direction)

To determine the percentage of adhesion separation by only measuring test results that had no more than 5% of the NE adhesive area separated.

At Point A where the NE connects to the pad, connect a cord to pull on the cable. Pull for 10 to 10.25 minutes, in a plane parallel to the NE pad and in a direction away from the center of the pad, with 10 to 11N (1.02 to 1.12kg) of force in the direction along the minor dimension of the pad. Set the height of the pulley so that the direction of pull shall be approximately co-planer with the plane of the connection point of the NE. The pull shall be performed by a cord connected to the NE at the cable connection point. See Figure 2 for the pull set up. The weights provide the required pull force. Start timer. At 10 mins, change direction of pull to y direction by rotating the pulley system 90 degrees as shown in Figure 2 - apply 10 to 11 N force at Point A in direction of y ray which is in a plane parallel to the pad.

Start timer. At 10 mins

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

F2 Labs

🇺🇸

Damascus, Maryland, United States

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