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A Randomized single-blind clinical study: The efficacy and safety of Daylight PDT and Red light PDT in the treatment of actinic keratosis

A Randomized single-blind clinical study: The efficacy and safety of Daylight PDT and Red light PDT in the treatment of actinic keratosis

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-INR-17013506
Enrollment
Unknown
Registered
2017-11-23
Start date
2017-12-01
Completion date
Unknown
Last updated
2017-11-27

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

Conditions

actinic keratoses

Interventions

Daylight-PDT Group:Daylight-PDT

Sponsors

Shanghai Skin Disease Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: (1) Clinical diagnosed with AK (OLSEN classification grade I, II, III), aged > 18 years; (2) All patients are unfit and reluctant to undergo surgery for any reasons, and volunteered to participate in the study and signed informed consent. Patents are willing to pay for the treatment, and agreed to take a picture of the skin lesions.

Exclusion criteria

Exclusion criteria: (1) Those who had ALA-PDT and any other studies that affect this study within 12 weeks ; (2) There are other facial diseases that may affect the efficacy evaluation, such as other photodermatosis; (3) Take phototoxic or photosensitizer within 8 weeks; (4) clinical and / or pathological prove that the tumor has invaded other organs or tissues; (5) Serious immunocompromised persons; (6) scar constitution; (7) Patients are known to have skin photosensitivity, porphyria, or allergies to ALA, light or lidocaine; (8) Persons are suffering from severe internal diseases, mental and mental illness, infectious diseases or pregnant or lactating women.

Design outcomes

Primary

MeasureTime frame
Complete clearance rate of AK lesions at month 1 after PDT;

Secondary

MeasureTime frame
New AKs during following up;Recurrence time of AK;Pain and pruritus score after and during treatment;Other side effects rate;

Countries

China

Contacts

Public ContactXiuli Wang

Shanghai Skin Disease Hospital

xlwang2001@aliyun.com+86 18017336663

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026