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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03697590
Other study ID # PDT with and without curettage
Secondary ID
Status Completed
Phase Phase 4
First received
Last updated
Start date June 1, 2017
Est. completion date December 20, 2017

Study information

Verified date June 2017
Source Bispebjerg Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Guidelines for photodynamic therapy (PDT) of actinic keratosis recommend pretreatment with curettage. The impact of curettage on the treatment effect is, however, not known. The present study aimed to evaluate whether daylight-PDT without curettage would reduce treatment effect compared to daylight-PDT with curettage.


Recruitment information / eligibility

Status Completed
Enrollment 25
Est. completion date December 20, 2017
Est. primary completion date December 20, 2017
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Multiple actinic keratosis on the forehead or scalp

Exclusion Criteria:

- Known allergy to methyl aminolevulinate

- Porphyria

- Pregnancy

- Lactation

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
No curettage
Standard PDT without curettage
Curettage
Standard PDT

Locations

Country Name City State
Denmark Bispebjerg Hospital Copenhagen NV DK

Sponsors (1)

Lead Sponsor Collaborator
Bispebjerg Hospital

Country where clinical trial is conducted

Denmark, 

Outcome

Type Measure Description Time frame Safety issue
Primary Complete lesion response rate Complete lesion response rate, was defined as the number of completely responding lesions divided by the total number of treated lesion in each field. Complete lesion response was defined as complete disappearance of the lesion both by palpation and visually. Treatment efficacy was evaluated 3 months after PDT
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