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临床试验/NCT05176015
NCT05176015已完成不适用

Randomized Controlled Trial on Nystagmus Assessment for Patients Consulting for Acute Vertigo in the Emergency Department With/Without Frenzel Lens With/Without Form: A Pilot Study

CHU de Quebec-Universite Laval5 个研究点 分布在 1 个国家目标入组 120 人开始时间: 2022年1月15日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
120
试验地点
5
主要终点
Rate of Nystagmus detection per participant

研究概览

简要总结

This pilot study is perfomed to validate and document faisability of the use of Frenzel lens and the use of a diagnostic algorithm for the assessment of a special sign (nystagmus) observe in the eyes of patients consulting in the emergency department (ED) for an acute episode of vertigo/dizziness/imbalance.

详细描述

This pilot study is a randomized controlled trial 2 by 2 design to allocated randomly the Frenzel lens and the diagnostic algorithm. There is no use of sham lens. The usual care opposed to the diagnostic algorithm will be questioned only on the perception of nystagmus by the clinician and the use of repositioning particles technique. The only blinding will be the patients about the use of the algorithm and the outcomes assessor about the use or not of Frenzel lens and the use or not of the diagnostic algorithm.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Diagnostic
盲法
Triple (Participant, Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 100 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • New episode of acute vertigo/dizziness/imbalance occuring during the 28 last days
  • Must be able to consent.

排除标准

  • No traumatic context before symptoms onset
  • No intoxication context
  • Glycemia ≤ 3,0 mmol/L
  • Only one participation is permitted
  • Not able to speak adequately in French or English.
  • Reachable for 3 month follow-up

研究组 & 干预措施

Frenzel Lens with Diagnostic Algorithm

Experimental

Frenzel lens will be applied on patients' eyes during different diagnostic maneuvers to assess if a nystagmus is present and if present describe its main characteristic.

Without mentioning to patient, the emergency physician will use a diagnostic algorithm inspired from the TiTrATE approach to interpret the nystagmus and propose the need or the irrelevance for neuro-imaging

干预措施: Frenzel Lens (Device)

Frenzel Lens with Diagnostic Algorithm

Experimental

Frenzel lens will be applied on patients' eyes during different diagnostic maneuvers to assess if a nystagmus is present and if present describe its main characteristic.

Without mentioning to patient, the emergency physician will use a diagnostic algorithm inspired from the TiTrATE approach to interpret the nystagmus and propose the need or the irrelevance for neuro-imaging

干预措施: Diagnostic Algorithm (Diagnostic Test)

Frenzel Lens without Diagnostic Algorithm

Experimental

Frenzel lens will be applied on patients' eyes during different diagnostic maneuvers to assess if a nystagmus is present and describe its main characteristics. No diagnostic algorithm will be used to interpret nystagmus.

干预措施: Frenzel Lens (Device)

No Frenzel Lens with Diagnostic Algorithm

Experimental

Nystagmus assessment in different manoeuvres is performed without the use of Frenzel lens.

Without mentioning to patient, the emergency physician will use a diagnostic algorithm inspired from the TiTrATE approach to interpret the nystagmus and propose the need or the irrelevance for neuro-imaging

干预措施: Diagnostic Algorithm (Diagnostic Test)

No Frenzel Lens and No Diagnostic Algorithm

No Intervention

The emergency physician is performing the assessment of nystagmus and its interpretation as usual. The Frenzel lens and the diagnostic algorithm are not used.

结局指标

主要结局

Rate of Nystagmus detection per participant

时间窗: Day 0

During eye examination, nystagmus will be characterized according to prominent direction of the fast phase (patients' left, patients' right, up, down, rotational),with their clinical setting or trigger. Overall rate of nystagmus detection by participant. (Rate of typical nystagmus for benign paroxysmal positional vertigo in the Dix-Hallpike maneuver or Supine Head Roll Test. Rate of nystagmus detection in the initial physical exam)

次要结局

  • Rate of acute stroke per participant(From day 0 to 12 weeks)
  • Rate of subsequent Emergency Department Visit for Vertigo/dizziness/imbalance per participant(From day 0 t0 12 weeks)
  • Adverse Events(From day 0 to 12 weeks)
  • Initial managment self appreciation of patient presenting in the ED for an acute episode of vertigo/dizziness/imbalance(Day 0)
  • Emergency Department Length of stay(Day 0, from triage time to Emergency Department departure (admission or home discharge))
  • Rate of specialised consultations for vertigo/dizziness/imbalance per participant(From day 0 to 12 weeks)
  • Rate of acute vertigo/dizziness/imbalance related hospitalisation per participant(From day 0 to 12 weeks)
  • Rate of symptomatic central lesion per participant(From day 0 to 12 weeks)
  • Rate of the use of Particles Repositioning Technique(Day 0)
  • Rate of Emergency Department Visit Return for Benign Paroxysmal Positional Vertigo according to Typical Nystagmus(From day 0 to 12 weeks)
  • Rate of neuro-imaging per participant(From day 0 to 12 weeks)
  • Rate of New Atrial Fibrillation(From day 0 to 12 weeks)
  • Rate of New Stroke at 12 weeks(At 12 weeks)

研究者

发起方
CHU de Quebec-Universite Laval
申办方类型
Other
责任方
Principal Investigator
主要研究者

Pierre La Rochelle

Chief Investigator

CHU de Quebec-Universite Laval

研究点 (5)

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