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临床试验/NCT02322164
NCT02322164已完成不适用

Psychophysical Correlates of Pain Reduction by Topical Analgesic Compounds

National Center for Complementary and Integrative Health (NCCIH)1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2014年12月19日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
40
试验地点
1
主要终点
Thermal sensory discrimination

研究概览

简要总结

Background:

  • Researchers are studying a topical (skin) cream that reduces pain. This is called an analgesic cream. They want to try a new test to better measure how well it works. Heat will be applied to the participants arms and they will judge the intensity of the temperatures. Researchers will compare the pain reduction from this cream to other pain relief treatments.

Objective:

  • To better measure the effects of a pain-relieving (analgesic) cream.

Eligibility:

  • Healthy volunteers ages 18 50.

Design:

  • There will be 2 study sessions.

  • Session 1 will be about 1.5 hours.

  • Participants will be screened with physical exam and urine drug test. They will answer medical and psychological questions.

  • Participants will have sensory testing.

  • A moisturizer will be put on their arms. A heating device will be placed on their arms. It gives heat pulses of about 2 seconds each. Some are warm and some are very hot. Participants will say how strong each pulse is. They can move away if it gets painful.

  • Then the pain-relieving cream will be put on one arm. The moisturizer will be put on the other. Participants will get more pulses and rate them. They will also get pairs of pulses and compare them.

  • Some participants will return for session 2 for 1 hour. They will receive similar sensory testing as in session 1.

详细描述

This study uses a new testing design to evaluate pain reduction from a pain-relieving cream. Sequences of heat stimuli will be applied to the participants arms and participants will be asked to judge the intensity of the temperatures they perceive. There are two study sessions. Session 1 involves eligibility screening and baseline sensory testing with and without the analgesic (pain-relieving) cream. Session 2 involves more sensory testing with the analgesic cream. The study population is 40 healthy volunteers aged 18 to 50.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Cross Sectional

入排标准

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

入选标准

  • 未提供

排除标准

  • 未提供

结局指标

主要结局

Thermal sensory discrimination

时间窗: One time point

次要结局

未报告次要终点

研究者

申办方类型
Nih
责任方
Sponsor

研究点 (1)

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