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Photodynamic Therapy Using Aminolevulinic Acid in Treating Patients With Skin Cancer

Investigation of the Effectiveness of Non-Coherent Blue Light in Intralesional Photodynamic of Basal Cell Carcinoma

Status
UNKNOWN
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00747903
Enrollment
20
Registered
2008-09-08
Start date
2008-02-29
Completion date
Unknown
Last updated
2014-01-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Non-melanomatous Skin Cancer

Keywords

basal cell carcinoma of the skin, recurrent skin cancer

Brief summary

RATIONALE: Photodynamic therapy uses a drug that becomes active when it is exposed to a certain kind of light. When the drug is active, tumor cells are killed. This may be an effective treatment against skin cancer. PURPOSE: This phase II trial is studying the side effects of photodynamic therapy using aminolevulinic acid and to see how well it works in treating patients with skin cancer.

Detailed description

OBJECTIVES: * To determine the safety and efficacy of intralesional photodynamic therapy using aminolevulinic acid and non-coherent blue light in patients with nodular basal cell carcinoma. OUTLINE: Patients undergo photodynamic therapy comprising intralesional injection of aminolevulinic acid followed by non-coherent blue light therapy over approximately 17 minutes. Patients may undergo re-treatment with photodynamic therapy 8 weeks later. Patients undergo photographic assessment of their skin lesions at baseline, 8 weeks, 16 weeks, and then at 1 and 2 years to evaluate healing time, clinical improvement, and side effects. Patients undergo biopsies of their skin lesions at 16 weeks and then at 1 and 2 years to confirm histological clearance.

Interventions

Sponsors

Laser and Skin Surgery Center of New York
Lead SponsorOTHER

Study design

Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
30 Years to No maximum
Healthy volunteers
No

Inclusion criteria

DISEASE CHARACTERISTICS: * Biopsy-proven basal cell carcinoma on the trunk or extremities * Tumor size ≤ 2 cm in diameter PATIENT CHARACTERISTICS: * Willing and able to comply with all follow-up requirements * Mentally competent * No active, localized, or systemic infections * Not immunocompromised * No coagulation disorder * No photosensitivity or allergy to sunlight * Not pregnant or nursing * No history of keloid formation * No history of cutaneous photosensitization, porphyria, hypersensitivity to porphyrins, or photodermatosis PRIOR CONCURRENT THERAPY: * No prior gold therapy * No prior radiotherapy to the trunk and extremities * More than 24 months since prior oral retinoids (e.g., isotretinoin or acitretin) or photosensitizing drugs (e.g., Declomycin®) * More than 1 year since prior collagen or other injections, Botox® injections, chemical peels, dermabrasion, or resurfacing procedures * More than 1 month since prior topical retinoid therapy * No concurrent aspirin or antioxidants * No concurrent anticoagulation medications

Design outcomes

Primary

MeasureTime frame
Safety
Efficacy

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026