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Tegaderm vs. Transpore Eye Tape for Eyelid Redness
N/A
Waitlist Available
Research Sponsored by Tufts Medical Center
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Surgeries scheduled for anesthesia of any duration
At least 18 years old
Must not have
Surgery in the prone position
Any surgery on the head, brain, neck, teeth, mouth, eyes, or face
Timeline
Screening 3 weeks
Treatment Varies
Follow Up immediately after tape removal
Awards & highlights
No Placebo-Only Group
Summary
This trial compares two types of medical tapes used to keep patients' eyes closed during surgery. It aims to find out which tape causes less eyelid irritation in patients undergoing anesthesia.
Who is the study for?
This trial is for adults over 18 who are scheduled for any surgery requiring anesthesia, except surgeries involving the head, neck, face, eyes or mouth. It's not for those with pre-existing eyelid redness or trauma, eyelid piercings, or anyone undergoing surgery in a prone position.
What is being tested?
The study aims to compare Tegaderm Eye Tape and Transpore Eye Tape to see if there's a difference in causing eyelid redness after anesthesia. Participants will be randomly assigned one of the two tapes during their procedure.
What are the potential side effects?
Potential side effects may include irritation at the tape application site leading to redness of the eyelids (eyelid erythema) following removal post-anesthesia.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
I am scheduled for surgery that requires anesthesia.
Select...
I am 18 years old or older.
Exclusion Criteria
You may be eligible for the trial if you check “No” for criteria below:Select...
I will have surgery lying on my stomach.
Select...
I have had surgery on my head, brain, neck, teeth, mouth, eyes, or face.
Select...
I have redness or injury on my eyelid.
Select...
I am under 18 years old.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ immediately after tape removal
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~immediately after tape removal
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
The proportion of eyelids with erythema at the end of surgery after removal of Tegaderm vs. Transpore
Secondary study objectives
Edema
Epidermal Change
Awards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
2Treatment groups
Experimental Treatment
Group I: Transpore RightExperimental Treatment1 Intervention
After general anesthesia is administered, Transpore will be placed on the right eye and Tegaderm will be placed on the left eye.
Group II: Tegaderm LeftExperimental Treatment1 Intervention
After general anesthesia is administered, Tegaderm will be placed on the left eye and Transpore will be placed on the right eye
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Tegaderm Eye Tape
2021
N/A
~170
Transpore Eye Tape
2021
N/A
~170
Research Highlights
Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
The most common treatments for eyelid redness include topical antibiotics, anti-inflammatory agents, and protective barriers like TegadermTM and Transpore®. Topical antibiotics, such as erythromycin, work by reducing bacterial load and preventing infection.
Anti-inflammatory agents, like corticosteroids, decrease inflammation and redness by suppressing the immune response. Protective barriers, such as TegadermTM and Transpore®, shield the skin from external irritants and help maintain a moist environment, promoting healing.
These treatments are crucial for patients with eyelid redness as they address the underlying causes of redness, reduce symptoms, and prevent complications.
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Find a Location
Who is running the clinical trial?
Tufts Medical CenterLead Sponsor
263 Previous Clinical Trials
264,303 Total Patients Enrolled
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- I will have surgery lying on my stomach.I have had surgery on my head, brain, neck, teeth, mouth, eyes, or face.I have redness or injury on my eyelid.I am under 18 years old.I am scheduled for surgery that requires anesthesia.I am 18 years old or older.You have piercings on your eyelids.
Research Study Groups:
This trial has the following groups:- Group 1: Tegaderm Left
- Group 2: Transpore Right
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
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