← Back to Search

Other

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
16,362 Total Patients Enrolled
~7 spots leftby Jun 2025