研究目的
Compare a conventional regimen (1 h ALA preincubation, followed by blue light), to a new modified regimen in which blue light is started immediately after ALA application to minimize pain during illumination.
研究成果
The modified PDT regimen is essentially painless, yet provides treatment efficacy similar to a conventional regimen.
研究不足
Although bilaterally controlled, the study was relatively small. Additional studies are recommended.
1:Experimental Design and Method Selection:
A clinical trial with a bilaterally controlled, intrapatient study design was conducted.
2:Sample Selection and Data Sources:
Eligible patients had at least 8 non-hypertrophic actinic keratoses (AK), with at least 4 lesions on each side of the face or scalp.
3:List of Experimental Equipment and Materials:
Topical 20% ALA solution (Levulan Kerastick), blue light (Blu-U, 10 mW/cm2).
4:2). Experimental Procedures and Operational Workflow:
4. Experimental Procedures and Operational Workflow: On one side of the body, blue light was started immediately and continued for either 30, 45, or 60 min. On the contralateral side, blue light began 1 h after ALA application and lasted 1000 sec.
5:Data Analysis Methods:
Pain was evaluated on a 0-10 scale. AK lesion counts were determined by clinical exam and photography.
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