A Randomized, Double-Blind, Placebo-Controlled, Parallel Group Phase III Study of the Efficacy, Tolerability and Safety of Ketoprofen Topical Patch, 20% (KTP) in the Treatment of Pain Associated With Tendonitis or Bursitis of the Shoulder, Elbow or Knee
试验速览
- 阶段
- 3 期
- 状态
- 终止
- 发起方
- 入组人数
- 381
- 试验地点
- 2
- 主要终点
- Average pain intensity during daily activities
研究概览
简要总结
The purpose of this study is to evaluate the effect of a ketoprofen topical patch on the pain associated with tendonitis or bursitis of the shoulder, elbow or knee
详细描述
This randomized, double-blind, placebo-controlled, parallel group study will be conducted in patients with tendonitis or bursitis of the shoulder, elbow or knee. Eligible patients will have tendonitis or bursitis or the shoulder, elbow or knee and will be randomized (1:1 ratio) to receive double-blind treatment with either the KTP or a matching placebo patch to be applied once daily for 21 days. Patients will return to the clinic for assessments on Day 3, Day 7, Day 14 and Day 21; a follow-up assessment will be conducted by telephone on Day 35. At each visit through Day 21, patients will rate their average pain intensity during daily activities and while at rest using the 11-point scale (range 0 to 10), and will rate their functional disability. Patients will also complete an electronic diary in which pain intensity and pain relief ratings will be recorded three times daily. The use of study treatment and rescue medication will be recorded in the diary each day. Ibuprofen will be provided as prn rescue medication.
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
- Double (Participant, Investigator)
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Males or females 18 years of age or older
- •Diagnosis of tendonitis or bursitis of the shoulder, elbow or knee
- •Meet pain entry criteria
- •Willing to discontinue use of any pain medication not provided by study
排除标准
- •Have tendonitis or bursitis secondary to a systemic inflammatory disease, calcification or requiring surgery
- •Have received corticosteroids in the 30 days preceding screening
- •Have a history or physical examination finding that is incompatible with safe participation in the study
- •Have a history or physical examination finding that is incompatible with study product use
- •Are taking medications or other substances contraindicated due to the nature of the study medication or the potential for drug interactions.
- •Are taking medications that may significantly affect renal function
研究组 & 干预措施
Ketoprofene
干预措施: Ketoprofen Topical Patch 20% (Drug)
Placebo
干预措施: Placebo (Other)
结局指标
主要结局
Average pain intensity during daily activities
次要结局
- Average pain intensity while at rest; use of prn rescue medication; patient's and physician's global assessments of study medication, MPI, Sleep