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Immunomodulator
Imiquimod cream for Actinic Keratosis
Phase 4
Waitlist Available
Research Sponsored by Medicis Global Service Corporation
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 day 14 of each treatment period
Awards & highlights
Study Summary
The purpose of this study is to determine the potential effect of topically applied 3.75% imiquimod cream on atrial ectopy in actinic keratosis (AK) patients. The primary endpoint is the change in the 24-hour supraventricular premature beat count. The secondary endpoint is the change in 24-hour supraventricular premature couplet and run counts and atrial fibrillation (% time); change in 24-hour mean heart rate; change in 24-hour ventricular premature beat count, ventricular premature couplet and run counts.
Eligible Conditions
- Actinic Keratosis
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ day 14 of each treatment period
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~day 14 of each treatment period
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Change in 24-hour supraventricular beat count
Secondary outcome measures
Change in 24-hour mean heart rate
Change in 24-hour supraventricular premature couplet and run counts and atrial fibrillation (% time)
Premature Cardiac Complex
Trial Design
2Treatment groups
Active Control
Placebo Group
Group I: Imiquimod creamActive Control1 Intervention
Group II: Placebo creamPlacebo Group1 Intervention
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Who is running the clinical trial?
Medicis Global Service CorporationLead Sponsor
11 Previous Clinical Trials
2,655 Total Patients Enrolled
Robert W Babilon, MS, MBAStudy DirectorGraceway Pharmaceuticals, LLC
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