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Corticosteroid

Laser vs Clobetasol for Lichen Sclerosus

Phase 3
Recruiting
Led By Clemens B Tempfer, MD
Research Sponsored by Ruhr University of Bochum
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 throughout study completion (3 months; for a total of 4 or 5 assessments, depending on group assignment)
Awards & highlights
Pivotal Trial
No Placebo-Only Group

Summary

Lichen sclerosus (LS) is a common autoimmune disease of the genital skin. It affects 1/900 women with an age peak in the sixth decade of life and is manifested by chronic inflammation of the genital, perineal, and perianal areas associated with itching, burning, pain, and soreness. In addition, LS is associated with an increased risk of vulvar cancer. Treatment options for LS include topical steroids such as clobetasol, immunomodulators such as tacrolimus, and non-ablative laser treatment. Although both treatments are well documented and used in clinical practice, direct comparative studies of the efficacy of topical corticosteroids versus laser treatment in women with LS are rare. For example, a PubMed literature search (search date 2021-03-14; search terms: lichen sclerosus, laser, corticosteroids, steroids, clobetasol, randomized) identified only a single randomized trial with limited power. Given the available evidence, further high-quality studies are needed to define the superiority/inferiority of the different available treatment options such as nonablative lasers and topical corticosteroids. Therefore, in this prospective, randomized, open-label, comparative study, treatment success after 3 courses of non-ablative treatment with CO2 laser every 14 days will be compared with treatment success after topical application of clobetasol 0.05% over 3 months (daily in the first month, every other day in month 2, and 3 times/week during month 3) at the time point 3 months after treatment initiation.

Eligible Conditions
  • Lichen Sclerosus

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~throughout study completion (3 months; for a total of 4 or 5 assessments, depending on group assignment)
This trial's timeline: 3 weeks for screening, Varies for treatment, and throughout study completion (3 months; for a total of 4 or 5 assessments, depending on group assignment) for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
Vulvar burning, itching, and pain
Secondary study objectives
Efficacy - Physician-scored rate of visual improvement (0-10)
Safety - Number and severity of side effects
Subjective overall improvement (0-10)
+1 more

Awards & Highlights

Pivotal Trial
The final step before approval, pivotal trials feature drugs that have already shown basic safety & efficacy.
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: Laser GroupExperimental Treatment1 Intervention
3 applications every 14 days of a non-ablative CO2 laser treatment
Group II: Clobetasol GroupActive Control1 Intervention
Treatment with clobetasol-0,05% over 3 months (month 1: daily, month 2: every other day, month 3: 3x per week)

Find a Location

Who is running the clinical trial?

Ruhr University of BochumLead Sponsor
168 Previous Clinical Trials
364,665 Total Patients Enrolled
Clemens B Tempfer, MDPrincipal InvestigatorRuhr-Universität Bochum / Marien Hospital Herne
6 Previous Clinical Trials
2,629 Total Patients Enrolled
~48 spots leftby Jan 2026