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Completed Phase 3 Interventional Results available

Safety and Effectiveness Study of Actinic Keratosis Treatment Following Cryosurgery

ClinicalTrials.gov ID: NCT00894647

Public ClinicalTrials.gov record NCT00894647. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 22, 2026, 3:54 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 3b Randomized, Double-blinded, Placebo-controlled, Multicenter, Efficacy and Safety Study of Imiquimod Cream Following Cryosurgery for the Treatment of Actinic Keratoses

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The objective of this study is to evaluate the efficacy and safety of imiquimod cream versus placebo cream when used after cryosurgery in the treatment of actinic keratoses (AKs).

Study identification

NCT ID
NCT00894647
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Graceway Pharmaceuticals, LLC
Industry
Enrollment
247 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
May 2009 (Type not available)
Primary completion
Feb 2010 (Actual)
Completion
Feb 2010 (Actual)
Last update posted
Aug 31, 2010

2009 – 2010

United States locations

U.S. sites
14
U.S. states
10
U.S. cities
14
Facility City State ZIP Site status
Dermatology Research Associates Los Angeles California 90045 —
Therapeutics Clinical Research San Diego California 92123 —
Spencer Dermatology & Skin Surgery Center Saint Petersberg Florida 33705 —
Palm Beach Dermatology West Palm Beach Florida 33401 —
MedaPhase, Inc. Newnan Georgia 30263 —
Evanston Northwestern Healthcare Skokie Illinois 60077 —
Skin Specialists PC Omaha Nebraska 68144 —
Academic Dermatology Association Albuquerque New Mexico 87106 —
DermResearchCenter of New York Stony Brook New York 11790 —
Wake Forest Univ School of Medicine Winston-Salem North Carolina 27157 —
Oregon Medical Research Center Portland Oregon 97223 —
DermResearch Inc. Austin Texas 78759 —
Dermatology Treatment and Research Center Dallas Texas 75230 —
Progressive Clinical Research San Antonio Texas 78229 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 4 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00894647, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Aug 31, 2010 · Synced Oct 22, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00894647 live on ClinicalTrials.gov.

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