Metabolites of Tear Fluid

NCT ID: NCT03389282

Last Updated: 2018-01-03

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Total Enrollment

30 participants

Study Classification

OBSERVATIONAL

Study Start Date

2013-11-01

Study Completion Date

2018-04-01

Brief Summary

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The pilot trial evaluates the use of modified Schirmer strips and is designed to evaluate inter-individual range of metabolites in tear film.

Detailed Description

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The variability of tear film metabolites should be investigated in a sample of ophthalmologists in preparation for a pilot study in patients eye diseases.

The easy accessibility of the tear fluid and the lack of invasiveness of the study make it promising and sensible to determine the concentration of various tear film metabolites. Because attention has so far focused primarily on the quantitative and qualitative analysis of tear film proteins, many metabolites have so far only been shown to be contained in tears.

However, before the suitability of the measured values as a predictive parameter of the ocular surface for pathologies can be examined and assessed, it is necessary to determine the scattering variables in a sample of healthy volunteers. Thus, reference areas are to be defined for later investigations in order to enable reliable case number planning thereafter.

Repeated determinations at different times and on different days make it possible in particular to detect a time-dependent relationship in view of the dynamic variability of the tear film. The functional significance of certain metabolites can not yet be assessed in the establishment phase. However, the data may provide important information for the interpretation of a later, planned feasibility study with diseased patients or the influence of applied eye drops.

Conditions

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Healthy Subjects

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Interventions

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Tear Sampling

comprehensive eye exam, Schirmer test, break-up time, tear sampling

Intervention Type DIAGNOSTIC_TEST

Eligibility Criteria

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Inclusion Criteria

* healthy subjects at age \> 18 years

Exclusion Criteria

* in the case of subjects with a mental disability or legal guardianship, due to possible conflicts for the caregivers, a data evaluation and recording should in principle be dispensed with.
* subjects who have had any eye drops within the last 4 weeks, e.g. lubricants were used
* subjects undergoing clinical examination for symptoms of wetting disorder or morphological changes related to eye disease
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Institute of Ophthalmic Research Tuebingen

UNKNOWN

Sponsor Role collaborator

Institute for Clinical Epidemiology and Applied Biometry Tuebingen

UNKNOWN

Sponsor Role collaborator

University Hospital Tuebingen

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Focke Ziemssen, MD

Role: PRINCIPAL_INVESTIGATOR

Center for Ophthalmology, University of Tuebingen

Locations

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University Eye Hospital

Tübingen, Baden-Wurttemberg, Germany

Site Status RECRUITING

Countries

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Germany

Central Contacts

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Focke Ziemssen, MD

Role: CONTACT

+49 7071 29 84762

Sascha Dammeier, PhD

Role: CONTACT

+49 7071 29 84955

Facility Contacts

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Focke Ziemssen, MD

Role: primary

0049 7071 29 84761

Other Identifiers

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AZ 277/2013BO2

Identifier Type: -

Identifier Source: org_study_id

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