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Sun Protection for Surgical Scar Healing
N/A
Recruiting
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
Patient is scheduled for a cutaneous excisional surgical procedure
Surgery performed on sunlight-exposed anatomical regions (head, face, neck, hairless scalp)
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 3-12 months
Awards & highlights
Study Summary
This trial will test whether sun protection affects the appearance of scars after surgery to repair defects from Mohs micrographic surgery.
Who is the study for?
This trial is for adults over 18 who are having skin surgery in sun-exposed areas like the head, face, or neck. They must be able to consent and come back for a follow-up. It's not for pregnant individuals, prisoners, those under 18, anyone unwilling to return after 3 months, people allergic to zinc sunscreen, or with collagen vascular disease.Check my eligibility
What is being tested?
The study tests if zinc sunscreen affects how surgical scars heal and look after Mohs surgery. It's a split-wound trial where one part of the scar gets sunscreen and the other doesn't. After three months, they'll check scar appearance using special scales and instruments.See study design
What are the potential side effects?
Possible side effects may include reactions at the site where the sunscreen is applied on half of the wound such as redness or irritation; however specific side effects will be monitored throughout the study.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
I am scheduled for a skin surgery to remove tissue.
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I had surgery on parts of my body that are often exposed to the sun.
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I am 18 years old or older.
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My skin wound was stitched up in a straight line.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 3-12 months
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~3-12 months
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Patient observer assessment score (POSAS)
Secondary outcome measures
Colorimeter measurement of wound vascularity and hyperpigmentation.
Trial Design
2Treatment groups
Experimental Treatment
Group I: Sunscreen ApplicationExperimental Treatment1 Intervention
The study participant will be instructed to start applying the sunscreen provided to them to the randomly assigned half of the wound (A or B).
Group II: No Suncreen ApplicationExperimental Treatment1 Intervention
The study participant will be instructed to not apply the sunscreen provided to them to the randomly assigned half of the wound (A or B).
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Who is running the clinical trial?
University of California, DavisLead Sponsor
911 Previous Clinical Trials
4,709,469 Total Patients Enrolled
5 Trials studying Surgical Wound
233 Patients Enrolled for Surgical Wound
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- I had surgery on parts of my body that are often exposed to the sun.I am unwilling or unable to return for a follow-up in 3 months.I am 18 years old or older.My skin wound was stitched up in a straight line.I am scheduled for a skin surgery to remove tissue.I am under 18 years old.I am willing to come back for follow-up visits.
Research Study Groups:
This trial has the following groups:- Group 1: Sunscreen Application
- Group 2: No Suncreen Application
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.
Frequently Asked Questions
These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
What is the current enrollment size of this trial?
"Affirmative, clinicaltrials.gov supports the conclusion that this research is actively seeking participants. The study was established on July 16th 2021 and has seen its most recent update take place August 3rd 2022. 50 individuals will be recruited from one location for participation in this trial."
Answered by AI
Does this medical research currently seek to recruit additional participants?
"Evidenced by the clinicaltrials.gov entry, this trial is presently seeking participants. It was originally made available on July 16th 2021 and modified most recently on August 3rd 2022."
Answered by AI
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