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临床试验/TCTR20230202004
TCTR20230202004Unknown3 期

The study of effectiveness of platelet-rich plasma (PRP) treatment for lichen planus pigmentosus (pilot study)

Institute of dermatology0 个研究点目标入组 15 人开始时间: 2023年2月2日最近更新:
适应症

试验速览

阶段
3 期
发起方
入组人数
15

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
18 Years 至 60 Years(—)
性别
All

入选标准

  • 1. Patients who were diagnosed with lichen planus pigmentosus, age 18 - 60 years
  • 2. Has facial LPP lesion for at least 6 months
  • 3. Histology confirmed LPP as evidenced by perivascular infiltrate, lichenoid reaction, melanophages and pigment pigmentation (melanin) accumulates under the epidermis and dermis.
  • 4. Patch test result is negative

排除标准

  • 1. Patients who are pregnant or breastfeeding
  • 2. Patients with a history of keloids, hypertrophic scars, herpes virus infection or skin disease around the lesion
  • 3. Patients with blood disorders, liver disease or patients receiving chemotherapy/ anticoagulants
  • 4. Patients with hyperpigmentation from other conditions, such as pigmented contact dermatitis, with positive patch test results, fixed drug eruption, lichenoid drug reaction, ochronosis, melasma, PIH, endocrinopathies, etc.
  • 5. Patients with a history of treatment using topical bleaching agents and lasers within 6 months prior to study participation.

研究者

发起方
Institute of dermatology

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