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临床试验/NCT05981261
NCT05981261招募中不适用

Comparing Pain Intensity and Discomfort in Patients With Parkinson´s Disease and Healthy Controls During Inducement of Mechanical, Thermal, and Chemical Experimental Pain

University of Aarhus2 个研究点 分布在 1 个国家目标入组 63 人开始时间: 2023年6月7日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
63
试验地点
2
主要终点
Ongoing pain (Pain in PD)

研究概览

简要总结

Study comparing pain intensity and discomfort in patients with Parkinson´s disease and healthy controls during inducement of mechanical, thermal, and chemical experimental pain

详细描述

Project: Inducing experimental muscle pain in healthy volunteers, patients with Parkinson's disease in levodopa treatment, and patients with Parkinson's disease with deep brain stimulation treatment

Research team:

  • Andrea S. Poulsen (PI), PhD-student, AU
  • Sophie Rosenkjær, PhD-student, AU
  • Lene Vase, Professor, AU
  • Nanna B. Finnerup, Professor, AUH
  • Mette Møller, Leading doctor, AUH
  • Erisela Qerama Montvilas, Clinical lector, AUH
  • Jan Rosner, Post-doc, AUH

Objective: Comparing induced pain levels in (1) healthy volunteers, (2) patients with Parkinson's disease in levodopa treatment, and (3) patients with Parkinson's disease with deep brain stimulation treatment

Participants: 21 healthy volunteers, 21 patients with Parkinson's disease in levodopa treatment, and 21 patients with Parkinson's disease with deep brain stimulation treatment will be recruited from the Department of Neurology at Aarhus University Hospital. Furthermore, recruitment sheets will be posted at Aarhus University Hospital, at Parkinsonforeningen's webpage (https://www.parkinson.dk/) and newsletter and in local newspapers. A power calculation for a Wilcoxcon-Mann-Whitney rank sum test (Three groups) determine 21 in three test groups is adequate (effect size= 0.8; 1-β=.80; α=.05).

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Other
盲法
None

入排标准

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

Ongoing pain (Pain in PD)

时间窗: After assessment of motor response latencies measures (15 minutes)

Pain in PD will be assessed by King´s Parkinson´s disease pain scale (KPPS)

Thermal induced heat pain

时间窗: Immediately after assessment of ongoing pain (15 minutes)

Thermal heat detection and pain thresholds will be measured following the standardized "Quantitative Sensory Testing" protocol

Ongoing pain (Clinical pain in daily life)

时间窗: After assessment of motor response latencies measure (15 minutes)

Intensity and discomfort of ongoing pain in gluteus medius muscle, tibialis anterior muscle, and infraspinatus muscle will be assessed by use of 11- point Numeric Rating Scale (NRS)

Mechanical induced pain

时间窗: Immediately after assessment of thermal induced heat pain (15 minutes)

Mechanical pain thresholds and suprathresholds will be measured by use of a handhold pressor algometer (Somedic, Hörby, Sweden) with a 1-cm2 probe placed on test muscle (gluteus medius muscle, tibialis anterior muscle, and infraspinatus muscle in a randomized order)

Chemical induced pain

时间窗: Immediately after assessment of mechanical pain (15 minutes)

Chemical pain will be induced by an injection of hypertonic saline (HS, 5,8% in 1 ml)

Ongoing pain (Sensory and affective verbal descriptions of pain and patient drawings)

时间窗: After assessment of motor response latencies measures (15 minutes)

Sensory and affective verbal descriptions of pain and patient drawings of pain size and distribution will be measured by use of the short-form McGill Pain Questionnaire (SF-MPQ).

次要结局

  • Motor response latencies measure(Prior to assessment of ongoing pain (3 minutes))

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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