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Tegaderm Vs. Transpore for Eye Protection During Anesthesia

NCT04918290 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 165

Last updated 2024-10-28

No results posted yet for this study

Summary

The purpose of this study is to compare the rate of eyelid erythema after anesthesia with the use of TegadermTM vs. the Transpore®. Our null hypothesis is that the rate of erythema will be similar between the two groups given there is no evidence currently to suggest otherwise

Conditions

  • Eyelid Erythema

Interventions

DEVICE

Tegaderm Eye Tape

Eye tape to protect the eye from corneal abrasions during surgery.

DEVICE

Transpore Eye Tape

Eye tape to protect the eye from corneal abrasions during surgery.

Sponsors & Collaborators

  • Tufts Medical Center

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
OTHER
Masking
QUADRUPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2021-06-11
Primary Completion
2024-04-17
Completion
2024-05-15
FDA Device
Yes

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04918290 on ClinicalTrials.gov