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treatment arm for Surgical Incisions (Cicatricell Trial)

N/A
Waitlist Available
Research Sponsored by University of Toledo Health Science Campus
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be between 18 and 65 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 8 weeks to 6 months
Awards & highlights

Cicatricell Trial Summary

This trial sought to determine the efficacy of Cicatricell cream in reducing scarring and improving wound appearance.

Eligible Conditions
  • Surgical Incisions

Cicatricell Trial Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~8 weeks to 6 months
This trial's timeline: 3 weeks for screening, Varies for treatment, and 8 weeks to 6 months for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Improved wound appearance
Manchester Scar Scale
Modified Vancouver Scar Scale
+1 more

Cicatricell Trial Design

2Treatment groups
Experimental Treatment
Active Control
Group I: treatment armExperimental Treatment1 Intervention
receive cicatricell cream
Group II: control armActive Control1 Intervention
to treatment

Find a Location

Who is running the clinical trial?

University of Toledo Health Science CampusLead Sponsor
40 Previous Clinical Trials
16,552 Total Patients Enrolled

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
Recent research and studies
clinicaltrials.govStudy
Clinical Trial To Study The Anti-scarring Effect Of Cicatricell
2015. "Clinical Trial To Study The Anti-scarring Effect Of Cicatricell". ClinicalTrials.gov. https://clinicaltrials.gov/ct2/show/NCT03020420.
All > Scar
~7 spots leftby May 2025
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