At a glance
ClinicalIndex Comparison RecordN/ACompleted· 20 enrolled
Drug / intervention
Medline NE Grounding Paddevice
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
The Purpose of This Study is to Verify the Performance of the Neutral Electrode (NE) Adhesives in Accordance With the Testing Specified in IEC 60601-2-2:2017, Section 201.15.101.7, Pull Test.
In Brief
An observational study evaluating Medline NE Grounding Pad for Adhesion of the Neutral Electrode 21pad. Completed, enrolled 20 participants across 1 site.
Detailed 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.
Study Details
Study Typeobservational
Allocation--
Masking--
Primary Purpose--
ConditionsAdhesion of the Neutral Electrode 21pad
CountriesUnited States
CollaboratorsF2 Labs
Timeline
N/ACompletedFinished
2023202420252026
First PostedMay 2022
Enrollment StartMay 2022
Primary CompletionJun 2022
TodayJul 2026
First PostedMay 17, 2022
Enrollment StartMay 30, 2022
Primary CompletionJun 10, 2022
TodayJul 2, 2026
Enrollment to primary: 10 daysPosted 4.1 years ago
Interventions
Medline NE Grounding Paddevice
Split Universal Grounding Pads