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Diagnostic Test
Nystagmus Assessment for Vertigo
N/A
Waitlist Available
Led By Pierre La Rochelle, MD, MSc
Research Sponsored by CHU de Quebec-Universite Laval
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
New episode of acute vertigo/dizziness/imbalance occuring during the 28 last days
Be older than 18 years old
Must not have
Not able to speak adequately in French or English.
Timeline
Screening 3 weeks
Treatment Varies
Follow Up from day 0 to 12 weeks
Awards & highlights
No Placebo-Only Group
Summary
This trial tests special glasses and a diagnostic method to help doctors better identify eye movements in patients with dizziness or balance issues in the emergency room.
Who is the study for?
This trial is for individuals who can consent and have experienced a new episode of acute vertigo, dizziness, or imbalance in the last 28 days. Participants must be able to speak French or English and be available for follow-up after 3 months. Those with trauma, intoxication before symptoms, or very low blood sugar levels cannot join.
What is being tested?
The study tests the use of Frenzel lenses and a diagnostic algorithm to assess nystagmus (a vision condition) in patients with acute vertigo visiting the emergency department. It's designed to see if these tools are practical and accurate in a real-world setting.
What are the potential side effects?
Since this trial involves diagnostic procedures rather than medications, traditional side effects like those seen with drugs are not expected. However, discomfort from wearing Frenzel lenses may occur.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
I have experienced new episodes of vertigo, dizziness, or imbalance in the last 28 days.
Exclusion Criteria
You may be eligible for the trial if you check “No” for criteria below:Select...
I cannot speak French or English well.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ from day 0 to 12 weeks
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~from day 0 to 12 weeks
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Rate of Nystagmus detection per participant
Secondary study objectives
Adverse Events
Emergency Department Length of stay
Initial managment self appreciation of patient presenting in the ED for an acute episode of vertigo/dizziness/imbalance
+10 moreAwards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
4Treatment groups
Experimental Treatment
Active Control
Group I: No Frenzel Lens with Diagnostic AlgorithmExperimental Treatment1 Intervention
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
Group II: Frenzel Lens without Diagnostic AlgorithmExperimental Treatment1 Intervention
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.
Group III: Frenzel Lens with Diagnostic AlgorithmExperimental Treatment2 Interventions
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
Group IV: No Frenzel Lens and No Diagnostic AlgorithmActive Control1 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.
Research Highlights
Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
Acquired Nystagmus is often treated using medications, physical therapy, and specialized lenses. Medications such as gabapentin and memantine work by stabilizing neural activity in the brain, which can reduce the involuntary eye movements.
Physical therapy, including vestibular rehabilitation, helps improve balance and coordination, which can mitigate symptoms. Frenzel lenses, used in diagnostic settings, enhance the visibility of nystagmus, allowing for more accurate diagnosis and tailored treatment plans.
These treatments are crucial as they help manage symptoms, improve quality of life, and provide a clearer understanding of the condition for both patients and healthcare providers.
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Who is running the clinical trial?
CHU de Quebec-Universite LavalLead Sponsor
172 Previous Clinical Trials
109,555 Total Patients Enrolled
Pierre La Rochelle, MD, MScPrincipal InvestigatorUniversite Laval
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- I cannot speak French or English well.I have experienced new episodes of vertigo, dizziness, or imbalance in the last 28 days.You did not experience any injury before the symptoms started.You are not under the influence of drugs or alcohol.Your blood sugar level is less than 3.0 mmol/L.
Research Study Groups:
This trial has the following groups:- Group 1: Frenzel Lens with Diagnostic Algorithm
- Group 2: Frenzel Lens without Diagnostic Algorithm
- Group 3: No Frenzel Lens with Diagnostic Algorithm
- Group 4: No Frenzel Lens and No Diagnostic Algorithm
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.