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临床试验/NCT06439004
NCT06439004已完成不适用

The Use of Quantitative Sensory Testing to Characterize Somatosensory Functionality

Universitaire Ziekenhuizen KU Leuven2 个研究点 分布在 1 个国家目标入组 20 人开始时间: 2024年9月12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
20
试验地点
2
主要终点
Inter-period reproducibility of QST

研究概览

简要总结

Pain has a significant impact on quality of life and poses an enormous burden on the healthcare system. The subjective nature of pain complicates its mapping and treatment. Quantitative Sensory Testing (QST) aims to characterize the somatosensory phenotype using calibrated stimuli and subjective thresholds. This set of procedures enables quantification of the somatosensory function in small fibers (thinly myelinated Aδ and unmyelinated C), as well as large fibers (thickly myelinated Aβ). In this way, sensory loss (hypoesthesia, hypoalgesia) or sensory gain (hyperesthesia, hyperalgesia, allodynia) can be detected.

In this study, the inter-period reproducibility of thirteen QST parameters will be determined on the dominant hand, right forearm, right flank and lower back of 20 healthy volunteers.

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

年龄范围
18 Years 至 25 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Voluntary written informed consent has been obtained prior to any screening procedures.
  • Subject is ≥ 18 years and ≤ 25 years of age.
  • Subject is a non-smoker for at least 6 months before the start of the study.
  • Subject has a body mass index (BMI) between 18-30 kg/m².
  • Subject is in good general health, based on medical history and vital signs.

排除标准

  • Subject has a history of any illness which, in the investigator's opinion, might confound the results of the study, including conditions which affect the normal somatosensory functionality.
  • Subject has eczema, scleroderma, psoriasis, dermatitis, or any other abnormality on the skin of the dominant hand, right forearm, right flank or lower back which, in the investigator's opinion, might interfere with the study assessments.
  • Subject is unable to refrain from drinking alcohol 24 hours prior to each study visit, is currently a user of drugs, or has a history of alcohol and/or drug abuse.
  • Subject is unable to refrain from drinking caffeinated beverages 24 hours prior to each study visit.
  • Subject has used concomitant drugs and/or treatments that may interfere, in the investigator's opinion, with the study results.
  • Subject is in a situation or has a condition which, in the investigator's opinion, may interfere with safe and optimal participation in the study.
  • Female subject who is pregnant, breast-feeding or intends to become pregnant or is of child-bearing potential and is not using an adequate contraceptive method.
  • Subject is participating in another trial which, in the investigator's opinion, might confound the results of the study.

结局指标

主要结局

Inter-period reproducibility of QST

时间窗: Interval of 7 - 21 days between both periods

Inter-period reproducibility of thirteen different QST parameters on the dominant hand, right forearm, right flank and lower back of healthy volunteers.

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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