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临床试验/NCT01245946
NCT01245946已完成2 期

Efficacy Comparison Study of Topical Aminolaevulinic Acid-Photodynamic Therapy Versus Adapalene Gel 0.1% Plus Doxycycline for Treatment of Moderate Acne Vulgaris. Randomized, Simple Blind, Controlled Trial.

Pontificia Universidad Catolica de Chile1 个研究点 分布在 1 个国家目标入组 46 人开始时间: 2010年10月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
已完成
入组人数
46
试验地点
1
主要终点
Lesion counts

研究概览

简要总结

  • Acne vulgaris is a common inflammatory skin disease that affects more than 85% of teens and some people may continue throughout adulthood.
  • Topical retinoids related to oral antibiotics are considered first-line treatment of moderate inflammatory acne.
  • Recently, photodynamic therapy (PDT) with a photosensitizer, 5-aminolevulinic acid (ALA) or methyl aminolevulinate (MAL), has proven useful in the management of inflammatory acne. Although progress has been made in the study of photodynamic therapy for acne, to date, no study has compared PDT with standard and well-validated pharmaceutical treatments and with the current recommended therapy for most types of acne combination therapy with a topical retinoid plus one or more antimicrobial agents.

Hypothesis

  • PDT with the photosensitizer ALA will be effective and safe for the treatment of moderate facial inflammatory acne.
  • The ALA-PDT is more effective than conventional therapy with oral antibiotics and topical retinoids in the treatment of moderate inflammatory acne with faster action at 12 weeks of follow-up.

详细描述

  • There will be a randomized, controlled, single blind comparison study of PDT with 5-aminolevulinic acid (ALA) 20% versus conventional therapy consisting of topical 0.1% adapalene plus doxycycline 100 mg/day orally in patients with moderate inflammatory acne.
  • Be sought from all patients written informed consent prior to study entry.
  • For sample size calculation, we assumed that the correlation is the same in both groups and is relatively low (0.01), the number of lesions per subject is equal in both groups with a mean of 100 and low variance, which take 1 control per case and that. Whereas the percentage of improvement in the control group is 0.6 and expected in the treatment group is 0.7 yields a sample size of 23 patients in the treatment group and 23 new controls.

Interventions:

Patients will be randomized to receive:

  1. ALA-PDT: In 23 patients applied 20% ALA solution in the affected area for 1.5 hours. Subsequently irradiated with noncoherent red light (lamp Waldmann PDT 1200; wavelength 590-700 nm) with irradiance of 70 mW/cm2 and total dose or fluence of 37 J/cm2 for 7-9 minutes. From the sixth week will begin nightly topical adapalene 0.1% gel.
  2. Standard therapy:

In 23 patients applied topical adapalene 0.1% gel at night for 12 weeks plus doxycycline 100 mg / day for 6 weeks.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Single (Outcomes Assessor)

入排标准

年龄范围
18 Years 至 30 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Men and women between 18 and 30 years of age with moderate inflammatory acne

排除标准

  • Those who have received any treatment for acne either topic in the last 3 months before and systemic (including ACO started) in the last 6 months of the study.
  • Patients who are pregnant or breastfeeding.
  • Patients with history of photosensitivity or autoimmune disease.
  • Patients with a history or active TB disease or HIV.
  • Patient refusal to participate in the study.

研究组 & 干预措施

Photodynamic therapy

Experimental

干预措施: Photodynamic therapy (Procedure)

Conventional therapy

Experimental

干预措施: Conventional therapy (Drug)

结局指标

主要结局

Lesion counts

时间窗: Twelve weeks

Be conducted by an investigator blinded to the interventions, count of inflammatory and non-inflammatory acne lesions at the start of treatment and controls at the sixth and twelfth week.

次要结局

  • Photographic scores, quality of life, adherence to treatment and global severity of acne(Twelve weeks)

研究者

申办方类型
Other

研究点 (1)

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