跳至主要内容
临床试验/JPRN-UMIN000042010
JPRN-UMIN000042010已完成未知

Registry of palmoplantar pustulosis (PPP) treatment patterns, disease burden and treatment outcomes in Japan - ProPuP

Janssen Pharmaceutical K.K.0 个研究点目标入组 400 人开始时间: 2020年10月5日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
入组人数
400

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

年龄范围
18years-old 至 ot applicable(—)
性别
All

入选标准

  • 未提供

排除标准

  • 1.are receiving, or have received within the past 3 months, anti-inflammatory or analgesic systemic therapy such as oral corticosteroid, DMARDs, non-steroidal anti-inflammatory drugs, opioids, PDE4 inhibitor, or biologics for any other indication (e.g., psoriasis, rheumatoid arthritis, ankylosing spondylitis, psoriatic arthritis, asthma) 2.have received an investigational drug (including investigational vaccines) or used an invasive investigational medical device within 3 months before the start of the study or the first data collection time point 3.are participating in an investigational study 4.are participating in another observational study for guselkumab (including a post-marketing surveillance study) 5.are unable to understand or sign a participation agreement/informed consent form 6.if the only treatment they have received for PPP has been antibiotics when the decision was made.

研究者

相似试验