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Proteomic and Metabolomic Lacrimal Fingerprint in Diverse Pathologies of the Ocular Surface

Proteomic and Metabolomic Lacrimal Fingerprint in Diverse Pathologies of the Ocular Surface

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04198740
Acronym
EML-MSO
Enrollment
300
Registered
2019-12-13
Start date
2020-02-01
Completion date
2035-01-01
Last updated
2026-04-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Allergic Conjunctivitis, Dry Eye Syndrome, Infectious Keratoconjunctivitis, Mucous Membrane Pemphigoid

Keywords

Lacrimal fingerprint, Metabolomics, Proteomics, Ocular surface

Brief summary

This study aims to obtain the lacrimal fingerprint for frequent pathologies of the ocular surface and establish a normative base for each of them.

Detailed description

This is an exploratory study. The investigators aim to: * Test and perfect a tear sample analysis technique by mass spectrometry with samples collected by Schirmer strips; * Obtain the lacrimal fingerprint for various pathologies of the ocular surface, notably different forms of dry eye syndrome, infectious keratitis/conjunctivitis, mucous membrane pemphigoid and allergic conjunctivitis, and establish a normative base for each of them. During regular clinics at the cornea service of the ophthalmology department of the CHUM (Centre Hospitalier de l'Université de Montréal), the investigators aim to recruit a few hundred patients with various pathologies of the ocular surface, notably different forms of dry eye syndrome, infectious keratitis/conjunctivitis, mucous membrane pemphigoid and allergic conjunctivitis, and collect a sample of their tears via Schirmer strip. A case report form will be completed for each patient, noting known ocular diagnoses and active topical ophthalmic medication. Schirmer strips will be sent in sterile tubes to UQAM (Université du Québec à Montréal)'s department of chemistry for analysis by mass spectrometry.

Interventions

DIAGNOSTIC_TESTTear sample collection via Schirmer strip and subsequent analysis by mass spectrometry

During regular consultations at the ophthalmology department of the CHUM, eligible patients will undergo a standard 5 minute Schirmer tear test. The Schirmer strips will serve as tear samples and will be sent to UQAM's Department of chemistry for mass spectrometry analysis.

Sponsors

Centre hospitalier de l'Université de Montréal (CHUM)
Lead SponsorOTHER
Université du Québec a Montréal
CollaboratorOTHER

Study design

Observational model
OTHER
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Patients with healthy corneas or suffering from one of these pathologies: Dry eye syndrome; Infectious keratitis and/or conjunctivitis; Mucous membrane pemphigoid; Allergic conjunctivitis.

Exclusion criteria

* Patients younger than 18 years old; * Patients incapable of giving informed consent.

Design outcomes

Primary

MeasureTime frameDescription
To obtain the metabolomic and proteomic fingerprint of the studied ocular surface pathologies5 yearsRaw data will be analysed with MarkerView software by Sciex to identify specific over- or under-expressed markers in these ocular pathologies.

Secondary

MeasureTime frameDescription
To objectify changes in metabolomic and proteomic profile associated with topical treatments taken by participants in this study5 yearsRaw data will be analysed with the same software to identify specific changes in proteomic and/or metabolomic expression associated with the topical treatments taken by participants in this study.

Countries

Canada

Contacts

CONTACTMarie-Claude Robert, MD, M.Sc
marie-claude.robert.2@umontreal.ca514-890-8278
CONTACTMarie-Catherine Tessier
marie-catherine.tessier.chum@ssss.gouv.qc.ca514-890-8000
PRINCIPAL_INVESTIGATORMarie-Claude Robert, MD, M.Sc

Centre hospitalier de l'Université de Montréal (CHUM)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 28, 2026