Clinical Trials Logo

Actinic Keratosis clinical trials

View clinical trials related to Actinic Keratosis.

Filter by:

NCT ID: NCT01787383 Completed - Actinic Keratosis Clinical Trials

A Simultaneous Treatment Regimen Compared to a Sequential Treatment Regimen With Ingenol Mebutate Gel 0.015% and 0.05% of Two Areas With Actinic Keratosis on Face/Scalp and Trunk/Extremities

Start date: February 2013
Phase: Phase 3
Study type: Interventional

The purpose of this trial is to evaluate the safety of a simultaneous treatment regimen compared to a sequential treatment regimen when two separate areas with AKs (one located on face/scalp and the other located on trunk/ extremities) are treated with ingenol mebutate gel

NCT ID: NCT01742663 Completed - Actinic Keratosis Clinical Trials

A Study Comparing Diclofenac Sodium Gel 3% to Solaraze® Gel 3% in the Treatment of Actinic Keratosis

Start date: October 2012
Phase: Phase 1
Study type: Interventional

The objective of this study is to compare the relative efficacy and safety of the test formulation diclofenac sodium gel 3% (Taro Pharmaceuticals Inc.) to the marketed formulation Solaraze® (diclofenac sodium) Gel 3% (Fougera Pharms) in the treatment of actinic keratosis. Both the test and reference formulations will also be compared to a placebo formulation to test for superiority.

NCT ID: NCT01735942 Withdrawn - Actinic Keratosis Clinical Trials

Ingenol Mebutate Compared to Cryotherapy for the Treatment of Skin Lesions

Start date: October 2012
Phase: Early Phase 1
Study type: Interventional

The purpose of this study is to find out the effectiveness of ingenol mebutate compared to cryotherapy (freezing of the tissue) for the treatment of face and scalp skin lesions.

NCT ID: NCT01703078 Completed - Actinic Keratosis Clinical Trials

Safety and Tolerability of Different Concentrations of an Ingenol Derivative Field Therapy in the Treatment of Actinic Keratosis

Start date: November 2012
Phase: Phase 1
Study type: Interventional

The purpose of this study is to determine if the new ingenol derivative gels are as safe as and as well tolerated as ingenol mebutate gel when applied to AK lesions on the forearm for two consecutive days.

NCT ID: NCT01686152 Completed - Actinic Keratosis Clinical Trials

Study Comparing Imiquimod Cream, 3.75% to Zyclara® (Imiquimod) Cream, 3.75% in the Treatment of Actinic Keratosis

Start date: September 2012
Phase: Phase 3
Study type: Interventional

To determine the comparability of the safety and efficacy of Imiquimod Cream, 3.75% and Zyclara (imiquimod) Cream, 3.75% (the reference listed drug) in subjects with actinic keratosis (AK) of the face or balding scalp. It will also be determined whether the efficacy of each of the two active treatments is superior to that of the Vehicle cream.

NCT ID: NCT01656226 Active, not recruiting - Actinic Keratosis Clinical Trials

Long Term Efficacy and Safety of Eryfotona AK-NMSC® in Patients With Actinic Keratosis

Start date: July 2012
Phase: Phase 4
Study type: Interventional

The purpose of this study is to assess the efficacy, safety and tolerability of Eryfotona AK-NMSC® topical application vs Sunscreen on cancerization field of actinic keratosis patients after 6 months of treatment.

NCT ID: NCT01611480 Completed - Actinic Keratosis Clinical Trials

Efficacy and Safety of a New Topical Formulation With Imiquimod (Limtop) Applied 1, 3 or 7 Times Weekly During 2 x 2 Weeks Treatment for Actinic Keratosis on the Head

Start date: n/a
Phase: Phase 2
Study type: Interventional

The aim is to evaluate efficacy and safety of three different dosing regimens of Limtop in a study involving 96 patients with actinic keratosis on the head or face.

NCT ID: NCT01600014 Completed - Actinic Keratosis Clinical Trials

Ingenol Mebutate Gel, 0.015% Repeat Use for Multiple Actinic Keratoses on Face and Scalp

Start date: May 2012
Phase: Phase 3
Study type: Interventional

The purpose of the study is to demonstrate that ingenol mebutate gel is efficacious in treating Actinic Keratoses (AKs) present 8 weeks after initial field treatment or emerging in a previously cleared field.

NCT ID: NCT01583816 Completed - Actinic Keratosis Clinical Trials

Dose-finding, Safety, Efficacy Trial of Topical Resiquimod in Patients With Multiple Actinic Keratosis Lesions

Start date: May 2012
Phase: Phase 2
Study type: Interventional

A Dose-Finding Study of Resiquimod Evaluating Safety and Efficacy in Patients with Multiple Actinic Keratosis Lesions

NCT ID: NCT01571336 Completed - Actinic Keratosis Clinical Trials

Photodynamic Therapy of Actinic Keratoses With Alacare®

Start date: April 2012
Phase: N/A
Study type: Observational

This study aims to collect data on the frequency of SCCs in the Alacare®-treated area during an interval of two years after Alacare®-PDT.