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2-Octyl Cyanoacrylate for Scar
N/A
Waitlist Available
Led By Daniel Eisen, MD
Research Sponsored by University of California, Davis
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 3 months
Awards & highlights
No Placebo-Only Group
Summary
This trial is testing a special medical glue called Dermabond on patients who have had skin surgeries on their head and neck. The glue is applied on top of the wound to help seal it and possibly improve how the scar looks. Researchers want to see if using this glue makes wound care easier and if patients prefer it over traditional stitches. Dermabond is known for its strong bonding, water-resistant properties, and good cosmetic outcomes.
Eligible Conditions
- Scar tissue
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 3 months
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~3 months
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Scar Assessment as measured by Patient Observer Scar Assessment Score (POSAS)
Width of Scar as measured using Trace-to-Tape Method
Secondary study objectives
Complications or Adverse Events from Treatment
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
Active Control
Group I: Layered Closure with 2-Octyl CyanoacrylateExperimental Treatment1 Intervention
One half of the wound will have a cutaneous layer of sutures (2 layers), as is standard of care, while the other half of the wound will have an additional layer of 2-octyl cyanoacrylate (3 layers).
Group II: Layered ClosureActive Control1 Intervention
One half of the wound will have a cutaneous layer of sutures (2 layers), as is standard of care, while the other half of the wound will have an additional layer of 2-octyl cyanoacrylate (3 layers).
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Who is running the clinical trial?
University of California, DavisLead Sponsor
939 Previous Clinical Trials
4,739,699 Total Patients Enrolled
Daniel Eisen, MDPrincipal InvestigatorUniversity of California, Davis
10 Previous Clinical Trials
577 Total Patients Enrolled
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Eligibility Criteria:
This trial includes the following eligibility criteria:- You are going to have a skin surgery on your face or neck that will require stitches to close.You must be at least 18 years old.You agree to come back for follow-up appointments.You can understand the study information and agree to participate on your own.If you are planning to have a skin surgery at the UC Davis Dermatology Clinic, you will be checked if you are eligible for the study.
Research Study Groups:
This trial has the following groups:- Group 1: Layered Closure
- Group 2: Layered Closure with 2-Octyl Cyanoacrylate
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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