跳至主要内容
临床试验/CTIS2024-510839-22-00
CTIS2024-510839-22-00招募中1 期

A Prospective Real-World Evidence Study Evaluating the Effects of Voltaren use on Mobility and Quality of Life - 300128

Haleon CH S.a.r.l.0 个研究点目标入组 195 人开始时间: 2024年3月8日最近更新:
适应症

试验速览

阶段
1 期
状态
招募中
发起方
入组人数
195

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 至 65+(—)
性别
All

入选标准

  • A Subject between the age of 40 and 85 years., •A subject with diagnosed knee mild/non-serious osteoarthritis, proven via radiological evidence collected within the last 3 years., •A subject with self-reported knee pain, with a score of = 40 mm = 70mm on the pain intensity visual analogue scale at the Screening Visit., •A subject willing to use Voltaren Gel for up to 3 weeks.

排除标准

  • A subject with confirmed rheumatologic disease, •A subject who has experienced trauma to the knee within the last 2 months that resulted in pain and/or swelling., •A subject that has been administered local steroids or other NSAIDs injections to the knee within the last 3 months., •A subject with recent history of major knee injury or surgery., •A subject with knee skin area pathological condition which prevents application of product to the skins. Conditions such as: open skin wounds, infections, inflammations, or exfoliative dermatitis conditions., •A subject who is pregnant, lactating or plan to be pregnant or lactating during the study.

研究者

发起方
Haleon CH S.a.r.l.

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