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临床试验/NCT03199417
NCT03199417终止2 期

Trial Evaluating multimOdal toPical Cream In CompArison to pLacebo (TOPICAL)

University of Michigan1 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2017年5月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
终止
入组人数
50
试验地点
1
主要终点
Change in pain visual analog scale (VAS) scores (0-10) from baseline

研究概览

简要总结

Randomized controlled trial regarding the efficacy of a multimodal topical analgesic, Multiprofen, in comparison to placebo cream treatment on knee pain and function in patients with knee osteoarthritis.

详细描述

Knee osteoarthritis (OA) is a disease with a high global burden, and multiple conservative treatment options are available. In addition to being a major source of disability osteoarthritis results in a significant economic burden as well. A study published in 2012 showed the 1-year physician, outpatient procedure, and hospitalization costs in patients with osteoarthritis more than double those patients without osteoarthritis in Ontario.

Conservative treatment options include topical and oral anti-inflammatory medications, weight loss, physiotherapy and intra articular cortisone and viscosupplementation injections. Unfortunately, commonly used treatments such as oral anti-inflammatory medications carry a significant systemic adverse effect on the gastrointestinal (GI) tract and hepatic and renal systems and intra articular cortisone have potential adverse effect on blood glucose control. For this reason, topical anti-inflammatory medications are popular yet are often ineffective. Unfortunately, topical anti-inflammatory medications have variable efficacy in relieving osteoarthritic knee pain and often only provide a moderate degree of pain relief.

In the setting of chronic pain various other topical modalities have been utilized. A systematic review of the literature identified commonly studied topical analgesics were nonsteroidal anti-inflammatory drugs followed by lidocaine, capsaicin, amitriptyline, glyceryl trinitrate, opioids, menthol, pimecrolimus, and phenytoin. Given the biological bases behind utilizing agents which target a variety of pain generators the investigators hypothesized that a combination of these would provide significant pain relief to patients affected by end stage knee osteoarthritis. For this reason, the investigators propose a trial evaluating utilizing multiple topical modalities for pain relief to provide support for the use of combination therapy in treating knee osteoarthritis. Results from this study will potentially improve the global health and economic burden through improvement in the management of knee osteoarthritis.

STUDY OBJECTIVES

Primary objective The primary objective of the trial will be to evaluate the efficacy of a multimodal topical analgesic, Multiprofen, in comparison to placebo cream treatment on patient reported pain relief utilizing a 11-point visual analog scale (VAS) measured from 0-10.

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
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

盲法说明

Patients will be randomized using a random number generator to either intervention. Interventions will be identically packaged and labeled either A or B by a pharmacist who will be uninvolved with the trial administration. Participants and study personnel will be blinded to the treatment groups.

入排标准

年龄范围
50 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • The inclusion criteria are:
  • adult men or women ages 50-80 years;
  • Diagnosis of symptomatic osteoarthritis of the knee based on clinical and radiographic criteria;
  • provision of informed consent.

排除标准

  • The exclusion criteria are:
  • patients with inflammatory osteoarthritis;
  • open wounds or sores over the knee joint;
  • patients that will likely have problems, in the judgment of the investigators, with maintaining follow-up;
  • Cases involving litigation.

研究组 & 干预措施

Multiprofen/interventional

Experimental

A multimodal topical cream treatment with Ketoprofen, Baclofen, Amitryptiline, and lidocaine in a carrier gel. This topical formulation has been in use commercially under the trade name "Multi-profen". This topical cream will be applied by the patient three times per day.

干预措施: Multiprofen (Drug)

Control/Placebo Group

Placebo Comparator

A identically packaged placebo cream treatment will be utilized in the control population.

干预措施: Placebo (Other)

结局指标

主要结局

Change in pain visual analog scale (VAS) scores (0-10) from baseline

时间窗: week 0, week 3, week 6, week 12

Measurement of change in patient reported pain score (VAS) at various follow up appointments. The scale is from 0-10, with 10 being the most pain.

次要结局

  • Change in Western Ontario and McMaster Universities Arthritis Index (WOMAC) scores from baseline(week 0, week 3, week 6, week 12)
  • Change in Range of motion (ROM) from baseline(week 0, week 3, week 6, week 12)

研究者

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

Neil Bakshi

Researcher

University of Michigan

研究点 (1)

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