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Photo-Therapy With a Topical Retinoid Versus Photo-therapy Alone for Actinic Keratoses
This study is ongoing, but not recruiting participants.
First Received: September 19, 2008   Last Updated: November 19, 2009   History of Changes
Sponsor: Northwestern University
Information provided by: Northwestern University
ClinicalTrials.gov Identifier: NCT00756288
  Purpose

Evaluating safety and efficacy of the use of topical retinoid with photodynamic therapy for the treatment of actinic keratoses.


Condition Intervention
Actinic Keratoses
Procedure: Topical retinoid and blue-light therapy with photosensitizing agent
Procedure: Photodynamic Therapy (PDT)

Study Type: Interventional
Study Design: Treatment, Randomized, Double Blind (Investigator, Outcomes Assessor), Active Control, Parallel Assignment, Safety/Efficacy Study
Official Title: A Randomized Controlled Paired Comparison of Photo-therapy With a Topical Retinoid Cream Pretreatment Versus PDT Alone for Actinic Keratoses

Further study details as provided by Northwestern University:

Primary Outcome Measures:
  • Live blinded rater and blinded photo rater analysis of areas at week 0 and week 6 for erythema, edema, crusting, ulceration, palpability, need to cease/delay treatment, and overall response in reduction of number of AKs. [ Time Frame: 6 weeks ] [ Designated as safety issue: No ]

Secondary Outcome Measures:
  • Subjects will assess pain, burning and itching on a scale of 0-3 at week 0, during retinoid treatment, during photo-therapy, one day after, and week 6. Also, principal investigator will evaluate adverse events at week 6. [ Time Frame: 6 weeks ] [ Designated as safety issue: Yes ]

Estimated Enrollment: 20
Study Start Date: August 2008
Estimated Study Completion Date: November 2009
Primary Completion Date: August 2009 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
1: Experimental
Topical retinoid and Light therapy with photosensitizing agent
Procedure: Topical retinoid and blue-light therapy with photosensitizing agent
Topical Retinoid - Apply to AKs for 4 weeks Photo-therapy with photosensitizing agent- Apply to AKs at week 4
2: Active Comparator
Light therapy with photosensitizing agent
Procedure: Photodynamic Therapy (PDT)
Photo-therapy with sensitizing agent - apply to AKs at week 4

Detailed Description:

Evaluating safety and efficacy of the use of topical retinoid with photodynamic therapy vs photodynamic therapy alone for the treatment of actinic keratoses.

  Eligibility

Ages Eligible for Study:   18 Years to 80 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria

  • Adults aged 18-80 years old
  • Subjects with AK lesions who will receive PDT
  • Subjects with AK lesions in two areas other than face and scalp each with a surface area of 10cm2 or greater and at least 3 clinically diagnosed non-hypertrophic AK lesions in each
  • Subjects in good health
  • Subjects with willingness and the ability to understand and provide informed consent

Exclusion Criteria

  • Subjects who are pregnant or lactating
  • Subjects with a history of cutaneous photosensitivity or porphyria, hypersensitivity to porphyrins, or photodermatosis
  • Subjects with use of photosensitizing drugs within 1 week of study start
  • Subjects with use of topical medications such as corticosteroids, alpha-hydroxyacids or retinoids 2 weeks before study entry
  • Subjects who received previous treatment of target AKs within 4 weeks
  • Subjects who are unable to understand the protocol or give informed consent
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00756288

Locations
United States, Illinois
Northwestern University, Department of Dermatology
Chicago, Illinois, United States, 60611
Sponsors and Collaborators
Northwestern University
Investigators
Principal Investigator: Murad Alam, MD Northwestern University, Department of Dermatology
Study Chair: Jenneé A Rommel, MD Northwestern Univeristy, Department of Dermatology
  More Information

No publications provided

Responsible Party: Northwestern University, Department of Dermatology ( Murad Alam, MD )
Study ID Numbers: MA-071508
Study First Received: September 19, 2008
Last Updated: November 19, 2009
ClinicalTrials.gov Identifier: NCT00756288     History of Changes
Health Authority: United States: Institutional Review Board

Keywords provided by Northwestern University:
Actinic Keratoses
Blue light therapy
photosensitizer
Retinoid

Additional relevant MeSH terms:
Photosensitizing Agents
Keratosis
Radiation-Sensitizing Agents
Skin Diseases
Therapeutic Uses
Physiological Effects of Drugs
Dermatologic Agents
Pharmacologic Actions

ClinicalTrials.gov processed this record on February 08, 2010