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Keratosis, Actinic clinical trials

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NCT ID: NCT00859105 Completed - Actinic Keratosis Clinical Trials

A Randomized, Double-Blind, Parallel-Group, Vehicle-Controlled Therapeutic Equivalence Study of Three Imiquimod Cream 5% Treatments for Patients With Actinic Keratosis

Start date: February 2008
Phase: Phase 3
Study type: Interventional

Treatment, Randomized, Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Placebo Control, Parallel Assignment, Bio-equivalence Study

NCT ID: NCT00852137 Completed - Actinic Keratosis Clinical Trials

A Study to Evaluate the Pharmacokinetics of PEP005 (Ingenol Mebutate) Gel, 0.05%, When Applied in a Maximal Use Setting to the Dorsal Aspect of the Forearm in Patients With Actinic Keratosis

Start date: March 2009
Phase: Phase 2
Study type: Interventional

This Phase II study is designed to evaluate the pharmacokinetics of PEP005 (ingenol mebutate) Gel, 0.05% when applied in a maximal use setting to the dorsal aspect of the forearm in patients with actinic keratoses

NCT ID: NCT00850811 Completed - Actinic Keratosis Clinical Trials

A Study to Evaluate the Photoirritation Potential of PEP005 (Ingenol Mebutate) Gel, 0.01% in Healthy Volunteers

Start date: February 2009
Phase: Phase 1
Study type: Interventional

This Phase 1 study is designed to determine the photoirritation potential of PEP005 Gel, 0.01% when application is followed by light exposure.

NCT ID: NCT00850681 Completed - Actinic Keratosis Clinical Trials

A Study to Evaluate the Photoallergic Potential of PEP005 (Ingenol Mebutate) Gel, 0.01% in Healthy Volunteers

Start date: February 2009
Phase: Phase 1
Study type: Interventional

This Phase 1 study is designed to determine the photoallergic potential of PEP005 Gel, 0.01% and it's vehicle on normal skin.

NCT ID: NCT00843323 Completed - Actinic Keratosis Clinical Trials

Photodynamic Therapy (PDT) Effect on Large Surface Photodamaged Skin

PDT
Start date: December 2008
Phase: N/A
Study type: Interventional

In this study, 26 patients were selected and included for full-face photodynamic therapy sessions. All patients presented signs of photoaging skin and multiple actinic keratosis. Photographs and Biopsies were taken before and after the procedure. Clinical and histological aspects as well as immunohistochemical aspects regarding neocollagen induction and tumor expression were evaluated.

NCT ID: NCT00829192 Active, not recruiting - Clinical trials for Carcinoma, Squamous Cell

Phase II AK Study in Organ Transplant Patients

Start date: November 2007
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine whether afamelanotide (CUV1647) is effective in reducing the number of actinic keratoses and squamous cell carcinomas developing in immune compromised organ transplant recipients, who are at particularly high risk, over a 24 month test period. The number of lesions formed on the head, hands and forarms will be monitored over this 24 month test period.

NCT ID: NCT00828568 Completed - Actinic Keratosis Clinical Trials

Bioequivalence Study of Two Imiquimod Cream 5%

Start date: June 2008
Phase: Phase 1
Study type: Interventional

The primary objectives are to establish the therapeutic equivalence of imiquimod cream 5%, manufactured by Taro Pharmaceuticals Inc. and Aldara (imiquimod) cream, manufactured by 3M, and to show superiority over vehicle in the treatment of AK. The secondary objective is to compare the adverse event (AE) profiles of the two creams.

NCT ID: NCT00814528 Withdrawn - Actinic Keratosis Clinical Trials

Photodynamic Therapy Mediated by Topical Application of 5- ALA for the Treatment of Actinic Keratoses

Start date: November 2007
Phase: N/A
Study type: Interventional

The purpose of this study is to compare the treatment of skin growths called actinic keratoses (AK) with 5-ALA PDT, an FDA-approved treatment, versus treatment with other conventionally used FDA-approved agents such as cryotherapy, Imiquimod, or 5-fluorouracil (5-FU).

NCT ID: NCT00786994 Completed - Actinic Keratoses Clinical Trials

The Efficacy and Tolerability of Oleogel-S-10 in Patients With Actinic Keratoses

Start date: October 2008
Phase: Phase 2
Study type: Interventional

In this study the impact of Oleogel-S-10 versus placebo on actinic keratoses over a treatment period of 3 months will be tested. Additionally, once and twice daily applications are tested.

NCT ID: NCT00777127 Completed - Actinic Keratosis Clinical Trials

Long-term Effects of Imiquimod and Diclofenac in Actinic Keratoses

LEIDA
Start date: December 2008
Phase: Phase 4
Study type: Interventional

This clinical trial serves the purpose to compare the long-term effects of a treatment of actinic keratosis - your skin disorder - using Aldara® 5% cream or Solaraze® 3% gel on the face or the scalp. In particular, it should be found out whether the healing effect of these two medications on the skin lesions (i.e. the damaged skin parts) can be maintained for a prolonged period.