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临床试验/NCT06948188
NCT06948188尚未招募不适用

Identification of Subpopulations of Patients With Cholinergic Urticaria Based on the Results of Infrared Exposure

University Hospital, Montpellier1 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2025年5月30日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
尚未招募
入组人数
50
试验地点
1
主要终点
Positive infrared test result

研究概览

简要总结

This study aims to identify subpopulations of patients with cholinergic urticaria based on their sensitivity to infrared (IR) radiation exposure. Cholinergic urticaria is a chronic inducible urticaria triggered by increased body temperature. The study seeks to determine whether infrared exposure can induce symptoms in a subset of patients and whether these patients exhibit specific clinical or epidemiological characteristics.

详细描述

Cholinergic urticaria is characterized by small pruritic papules triggered by exercise, emotions, hot environments, or hot food and beverages. The pathophysiology remains unclear, but one hypothesis is that a central temperature increase plays a key role. A pilot study conducted at university hospital center (CHU) of Montpellier found that infrared exposure triggered symptoms in some patients with cholinergic urticaria. The infrared source was the same as that commonly used in photobiological tests.

The objective of this study is to identify the proportion of patients who develop cholinergic urticaria when exposed to infrared light. the investigators then aim to determine whether these patients have specific clinical or epidemiological characteristics that would allow them to be classified as a distinct subgroup of cholinergic urticaria and to assess whether sensitivity to infrared light is a prognostic marker of disease severity. Furthermore, measuring the core temperature of all patients during infrared light exposure will help determine whether patients sensitive to infrared light experience a greater increase in core temperature during the IR test. This would support the hypothesis that an increase in core temperature is responsible for triggering cholinergic urticaria flare-ups in this subgroup.

A better understanding of this condition and the identification of different subgroups could ultimately, with additional studies, allow for a personalized approach to patient management based on the cholinergic urticaria subgroup and each subgroup's sensitivity to different treatments.

研究设计

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

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

  • •Adults ≥ 18 years old
  • •Cholinergic urticaria diagnosed based on the diagnostic criteria published in 2016 (Magerl et al) : pruritic micropapules triggered by active or passive exposure to heat.
  • •Exercise test performed within the 6 months prior to inclusion.

排除标准

  • •Patients on H1 antihistamines within 72 hours before infrared exposure test
  • •Patients on any other specific treatment for cholinergic urticaria within a period of 5 plasma half-lives before infrared exposure test
  • •Patients with exercise-induced anaphylaxis (diet-induced or not)
  • •Patients with severe forms of cholinergic urticaria: angioedema, respiratory manifestations or anaphylaxis
  • •Participants who have reached the maximum compensation amount for their participation in research studies.
  • •Lack of consent (adults, non-emancipated minors, individuals unable to express consent, research conducted in emergency situations, etc.).
  • •Not being affiliated with or a beneficiary of a French social security scheme.
  • •Protected adults (under guardianship, curatorship, or judicial protection).
  • •Individuals participating in another research study with an ongoing exclusion period.
  • •Subjects deprived of liberty (Art. L. 1121-6) (by judicial or administrative decision, or involuntary hospitalization).
  • •Pregnant or breastfeeding women.
  • •Subjects who cannot read and/or write.

研究组 & 干预措施

Adult patients (> 18 years) with cholinergic urticaria

Experimental

Patient followed at Montpellier University Hospital with a diagnosis of cholinergic urticaria based on diagnostic criteria published in 2016 (Magerl et al): pruritic micropapules triggered by active or passive exposure to heat within 6 months following an exercise challenge test

干预措施: Infrared exposure test (Diagnostic Test)

结局指标

主要结局

Positive infrared test result

时间窗: During the 3 minutes of exposure to infrared light and the following 10 minutes.

the proportion (en percentage) of patients with cholinergic urticaria who develop urticarial lesions following infrared exposure.

次要结局

  • Comparison of age between patients with a positive and a negative infrared test(Baseline)
  • Comparison of age of onset of cholinergic urticaria, between patients with a positive and a negative infrared test(Baseline)
  • Comparison of sex between patients with a positive and a negative infrared test(Baseline)
  • Comparison of history of atopy between patients with a positive and a negative infrared test(Baseline)
  • Comparison of associated chronic urticaria, between patients with a positive and a negative infrared test(Baseline)
  • Comparison of cholinergic urticaria activity score,between patients with a positive and a negative infrared test(Baseline)
  • Comparison of triggering factors between patients with a positive and a negative infrared test(Baseline)
  • Comparison of treatment effectiveness (between patients with a positive and a negative infrared test(Baseline)
  • Comparison of time to onset of cholinergic urticaria (exercise) between patients with a positive and a negative infrared test(Baseline)
  • Comparison of time to onset of cholinergic urticaria (infrared) between patients with a positive and a negative infrared test(Baseline)
  • Comparison of maximum core temperature between patients with a positive and a negative infrared test(Baseline)
  • Comparison of average core temperature between patients with a positive and a negative infrared test(Baseline)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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