跳至主要内容
临床试验/NCT02955576
NCT02955576Unknown不适用

Efficacy of Microneedle Patch on Topical Ointment Treatment of Psoriasis

The Catholic University of Korea2 个研究点 分布在 1 个国家目标入组 20 人开始时间: 2016年9月最近更新:
适应症

试验速览

阶段
不适用
入组人数
20
试验地点
2
主要终点
The improvement of psoriasis

研究概览

简要总结

The purpose of this study is to evaluate the efficacy of microneedle patch on the psoriatic plaques.

详细描述

As a novel minimally invasive approach, microneedle-mediated transdermal drug delivery has received increased attention. Microneedle patch effectively penetrates the skin barrier of the stratum corneum and create efficient pathways for the delivery of drugs.

A randomized controlled trial based on split-body was planned to evaluate the efficacy of enhanced transdermal delivery of topical agent by hyaluronic acid (HA)-fabricated microneedle patch in psoriatic plaques. Six psoriatic plaques in a patient will be randomized to either microneedle HA patch, patch, or control groups. Patch group is planned for rule out the occlusion effect of patches. All lesions will be treated with topical agent and patches daily for 2-week period. The severity of psoriasis will be grated with modified PASI score and the clinical improvement will be assessed as % from baseline every week. Overall 20 patients with 120 psoriatic plaques will be enrolled.

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
19 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Age: older than 19
  • A patient with psoriasis
  • A patient with symmetrical psoriatic lesions
  • A patient with the willingness to comply with the study protocol during the study period and capable of complying with it
  • A patient who signed the informed consent prior to the participation of the study and who understands that he/she has a right to withdrawal from participation in the study at any time without any disadvantages

排除标准

  • Age: lower than 20
  • A pregnant or lactating patient
  • A patient who cannot understand the study or who does not sign the informed consent

结局指标

主要结局

The improvement of psoriasis

时间窗: Baseline, 1 week, 2 weeks

The severity of psoriasis will be graded with modified PASI score, and the improvement will be assessed as % from baseline by using a computer program.

次要结局

  • The adverse effects of microneedle patch(Baseline, 1 week, 2 weeks)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Jung Min Bae

Clinical Assistant Professor

The Catholic University of Korea

研究点 (2)

Loading locations...

相似试验