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Clinical Trials/NCT01482104
NCT01482104
Completed
Not Applicable

A Randomized Controlled Blinded Multi-centre Study of Photodynamic Therapy With Methyl-aminolevulinate Comparing a Simplified Regime With the Approved Regime in Patients With Clinical Low-risk Superficial and Nodular Basal Cell Carcinoma.

Norwegian University of Science and Technology9 sites in 1 country277 target enrollmentJune 2012

Overview

Phase
Not Applicable
Intervention
MAL-PDT re-treatment
Conditions
Skin Neoplasms
Sponsor
Norwegian University of Science and Technology
Enrollment
277
Locations
9
Primary Endpoint
lesions response rate
Status
Completed
Last Updated
8 years ago

Overview

Brief Summary

Basal cell carcinoma (BCC) is the most common malignant skin lesion in white adults. It is a slow-growing tumour which despite low metastatic potential may cause significant local tissue destruction and patient morbidity. Methyl aminolevulinate cream plus photodynamic therapy (MAL-PDT) for BCC is currently approved for a procedure using 2 treatment sessions 1 week apart. This procedure is considered quite time- and resource-consuming. Introducing a single treatment session, with a new PDT session for treatment failures after 3 months, might represent an attractive simplification.

This randomised controlled single-blinded multi-centre study primarily aims to compare BCC lesion response rate of two treatment schedules: (a) 1 single treatment of Metvix-PDT with re-treatment of non-complete responders by 3 months, and (b) the usual schedule of 2 standard Metvix(R) PDT treatments 1 week apart.

Secondary objectives are to investigate the treatment response in relation to clinical and histological tumour characteristics such as tumour thickness, subtype and immunohistochemical markers.

Registry
clinicaltrials.gov
Start Date
June 2012
End Date
October 2017
Last Updated
8 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • male/female above 18 years of age
  • written informed consent
  • 1 or more primary histologically verified BCC, clinically assessed as of either superficial of nodular type

Exclusion Criteria

  • pregnancy
  • breastfeeding
  • Gorlin's syndrome
  • porphyria
  • xeroderma pigmentosum
  • history of arsenic exposure
  • known allergy to MAL
  • concomitant treatment with immunosuppressive medication
  • physical or mental conditions that most likely will prevent patients attending follow-up sessions

Arms & Interventions

MAL-PDT re-treatment

1 treatment of MAL-PDT with re-treatment of non-complete responders

Intervention: MAL-PDT re-treatment

usual MAL-PDT

2 MAL-PDT treatments 1 week apart

Intervention: usual MAL-PDT

Outcomes

Primary Outcomes

lesions response rate

Time Frame: 3 years

Number of lesions in clinical complete response at follow-up

Study Sites (9)

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