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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT05749094
Other study ID # 20201890
Secondary ID
Status Not yet recruiting
Phase
First received
Last updated
Start date March 2024
Est. completion date August 2027

Study information

Verified date September 2023
Source Hopital du Sacre-Coeur de Montreal
Contact Jean-Paul Makhzoum, MD
Phone 5143382222
Email jean-paul.makhzoum@umontreal.ca
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The objectives of this observational cohort study are : 1. To assess the ability of optic nerve (ON), optic nerve sheath diameter (ONSD) and optic nerve sheath thickness (ONST) measured by ultrasound to predict Giant Cell Arteritis. 2. To evaluate changes in ON, ONSD, ONST measurements in patients with confirmed GCA after three months of therapy 3. To assess dynamic changes in ON, ONSD, ONST measurements in patients with relapsing GCA


Description:

Giant Cell Arteritis is the most common primary vasculitis in adult patients. GCA is difficult to diagnose, and no single test allows perfect classification of GCA. Imaging in GCA such as high resolution ultrasound is gaining populatity and allows identification of patients that would have been otherwise missed. Recently, optic nerve sheath enhancement on MRI has been described and associated with the presence of GCA. Evaluation of the optic nerve and optic nerve sheath using ultrasound is easy to perform but has never been assessed in GCA. Objectives: 1. To assess the ability of optic nerve (ON), optic nerve sheath diameter (ONSD) and optic nerve sheath thickness (ONST) measured by ultrasound to predict Giant Cell Arteritis. 2. To evaluate changes in ON, ONSD, ONST measurements in patients with confirmed GCA after three months of therapy 3. To assess dynamic changes in ON, ONSD, ONST measurements in patients with relapsing GCA


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 300
Est. completion date August 2027
Est. primary completion date August 2025
Accepts healthy volunteers
Gender All
Age group 50 Years to 95 Years
Eligibility Inclusion Criteria: - Adult patients referred to our fast-track vasculitis clinic with a clinical suspicion of new-onset GCA. - Must have a duration of glucocorticoid treatment of less than 14 days. - Must sign informed consent - Participation must be able to attend a 3 month follow-up visit, and in those with GCA, longitudinal clinic visits Exclusion Criteria: - Chronic use of immunosupressive therapy or glucocorticoids for more than 14 days - Pre-existing known retinal or optic nerve disease

Study Design


Related Conditions & MeSH terms


Intervention

Diagnostic Test:
Optic nerve ultrasound
The patients are examined in a supine relaxed position. The probe is gently placed on the closed eyelid with a standard ultrasound gel and adjusted to a suitable angle to display the optic nerve entry into the eyeball. Measurements are done 3mm distal to the posterior aspect of the ocular globe. Ultrasosonographic 14L5 probe is used with a safe thermal index, mechanical index and intensity limit. All patients will also undergo a bedside fundoscopic examination. Official ophthalmology consultation will be requested in patients with visual symptoms or abnormal fundoscopy.

Locations

Country Name City State
Canada Centre Hospitalier de Lanaudiere Joliette Quebec
Canada Vasculitis Clinic, Hopital du Sacre-Coeur de Montreal Montreal Quebec
Canada Centre Hospitalier de l'Université de Montréal Montréal Quebec
Canada Hopital Laurentien Sainte-Agathe-des-Monts Quebec

Sponsors (1)

Lead Sponsor Collaborator
Hopital du Sacre-Coeur de Montreal

Country where clinical trial is conducted

Canada, 

Outcome

Type Measure Description Time frame Safety issue
Primary Comparison of ON, ONSD, ONDT measurements in participants with and without GCA Baseline
Secondary In participants with GCA, evaluate ON, ONSD, ONDT measurement changes while on therapy. 3 months after baseline visit
Secondary In participants with suspected GCA relapse, evaluate ON, ONSD, ONDT measurement changes From month 3 to month 24 (following baseline visit)
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